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- [1] Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population[J]. Journal of Human Genetics, 2005, 50 : 347 - 352Shweta Singh论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringToshimitsu Suzuki论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringAkira Uchiyama论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringSatoko Kumada论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringNobuko Moriyama论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringShinichi Hirose论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringYukitoshi Takahashi论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringHideo Sugie论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringKoichi Mizoguchi论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringYushi Inoue论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringKazue Kimura论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringYukio Sawaishi论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringKazuhiro Yamakawa论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and BioengineeringSubramaniam Ganesh论文数: 0 引用数: 0 h-index: 0机构: Indian Institute of Technology,Department of Biological Sciences and Bioengineering
- [2] Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population[J]. JOURNAL OF HUMAN GENETICS, 2005, 50 (07) : 347 - 352Singh, S论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanSuzuki, T论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanUchiyama, A论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanKumada, S论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanMoriyama, N论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanHirose, S论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanTakahashi, Y论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanSugie, H论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanMizoguchi, K论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanInoue, Y论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanKimura, K论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanSawaishi, Y论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanYamakawa, K论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, JapanGanesh, S论文数: 0 引用数: 0 h-index: 0机构: RIKEN, Brain Sci Inst, Neurogenet Lab, Wako, Saitama 3510198, Japan
- [3] Compound heterozygosity for novel variations of the NHLRC1 Gene in a family with Lafora disease[J]. CLINICAL NEUROLOGY AND NEUROSURGERY, 2022, 218Tang, Xinghua论文数: 0 引用数: 0 h-index: 0机构: Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai, Peoples R ChinaLi, Xinjuan论文数: 0 引用数: 0 h-index: 0机构: Yangpu Daqiao Community Hlth Serv Ctr, Dept Gen Med, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai, Peoples R ChinaChen, Yuncan论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai, Peoples R ChinaWu, Dongyan论文数: 0 引用数: 0 h-index: 0机构: Fudan Univ, Huashan Hosp, Dept Neurol, Shanghai, Peoples R China Shanghai Jiao Tong Univ, Sch Med, Xinhua Hosp, Dept Neurol, Shanghai, Peoples R China
- [4] Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene[J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 2013, 325 (1-2) : 170 - 173Kecmanovic, Miljana论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Fac Biol, Belgrade 11000, Serbia Univ Belgrade, Fac Biol, Belgrade 11000, SerbiaJovic, Nebojsa论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Clin Ctr Serbia, Sch Med, Clin Neurol & Psychiat Children & Youth, Belgrade 11000, Serbia Univ Belgrade, Fac Biol, Belgrade 11000, SerbiaCukic, Mirjana论文数: 0 引用数: 0 h-index: 0机构: Clin Ctr Montenegro, Neurol Clin, Podgorica 81000, Montenegro Univ Belgrade, Fac Biol, Belgrade 11000, SerbiaKeckarevic-Markovic, Milica论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Fac Biol, Belgrade 11000, Serbia Univ Belgrade, Fac Biol, Belgrade 11000, SerbiaKeckarevic, Dusan论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Fac Biol, Belgrade 11000, Serbia Univ Belgrade, Fac Biol, Belgrade 11000, SerbiaStevanovic, Galina论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Clin Ctr Serbia, Sch Med, Clin Neurol & Psychiat Children & Youth, Belgrade 11000, Serbia Univ Belgrade, Fac Biol, Belgrade 11000, SerbiaRomac, Stanka论文数: 0 引用数: 0 h-index: 0机构: Univ Belgrade, Fac Biol, Belgrade 11000, Serbia Univ Belgrade, Fac Biol, Belgrade 11000, Serbia
- [5] NOVEL MUTATIONS IN EPM2A AND NHLRC1 WIDEN THE SPECTRUM OF LAFORA DISEASE[J]. EPILEPSIA, 2010, 51 : 138 - 139Lesca, G.论文数: 0 引用数: 0 h-index: 0机构: Serv Genet Moleculaire & Clin, Lyon, France IDEE, Lyon, France Serv Genet Moleculaire & Clin, Lyon, FranceBoutry-Kryza, N.论文数: 0 引用数: 0 h-index: 0机构: Univ Lyon 1, Hosps Civils Lyon, Serv Genet, F-69365 Lyon, France Serv Genet Moleculaire & Clin, Lyon, Francede Toffol, B.论文数: 0 引用数: 0 h-index: 0机构: CHU Bretonneau, Serv Neurol, F-37044 Tours, France Serv Genet Moleculaire & Clin, Lyon, FranceMilh, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants La Timone, Serv Neurol Pediatr, Marseille, France Serv Genet Moleculaire & Clin, Lyon, FranceSteschenko, D.论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Hop Enfants, Vandoeuvre Les Nancy, France Serv Genet Moleculaire & Clin, Lyon, FranceLemesle-Martin, M.论文数: 0 引用数: 0 h-index: 0机构: Hop Gen, Laboratoire Explorat Syst Nerveux, Dijon, France Serv Genet Moleculaire & Clin, Lyon, FranceMaillard, L.论文数: 0 引用数: 0 h-index: 0机构: Univ Nancy, Serv Neurol, Hop Cent, Ctr Rech Automat Nancy,UMR 7039,CNRS, Nancy, France Serv Genet Moleculaire & Clin, Lyon, FranceFoletti, G.论文数: 0 引用数: 0 h-index: 0机构: Inst Lavigny, Dept Neurol, Geneva, Switzerland Serv Genet Moleculaire & Clin, Lyon, FranceRudolf, G.论文数: 0 引用数: 0 h-index: 0机构: Hopitaux Univ Strasbourg, Serv Neurol, Strasbourg, France Serv Genet Moleculaire & Clin, Lyon, FranceNielsen, J. E.论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Inst Cellular & Mol Med, Neurogenet Sect, Copenhagen, Denmark Serv Genet Moleculaire & Clin, Lyon, FranceRogvi-Hansen, B. A.论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Rigshosp, Dept Neurol, Copenhagen, Denmark Serv Genet Moleculaire & Clin, Lyon, FranceErdal, J.论文数: 0 引用数: 0 h-index: 0机构: Copenhagen Univ Hosp, Rigshosp, Dept Neurol, Copenhagen, Denmark Serv Genet Moleculaire & Clin, Lyon, FranceMancini, J.论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants La Timone, Serv Neurol Pediatr, Marseille, France Serv Genet Moleculaire & Clin, Lyon, FranceThauvin-Robinet, C.论文数: 0 引用数: 0 h-index: 0机构: Hop Enfant, CHU Dijon, Ctr Genet, Dijon, France Serv Genet Moleculaire & Clin, Lyon, FranceRrabet, A. M.论文数: 0 引用数: 0 h-index: 0机构: EPS Charles Nicolle, Serv Neurol, Tunis, Tunisia Serv Genet Moleculaire & Clin, Lyon, FranceVille, D.论文数: 0 引用数: 0 h-index: 0机构: Hop Femme Mere Enfant, Serv Neuropediatrie, Lyon, France Serv Genet Moleculaire & Clin, Lyon, FranceSzepetowski, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Aix Marseille 2, Inst Neurobiol Mediterranee, INMED, INSERM,UMR901, Marseille, France Serv Genet Moleculaire & Clin, Lyon, FranceRaffo, E.论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Hop Enfants, Vandoeuvre Les Nancy, France Serv Genet Moleculaire & Clin, Lyon, FranceHirsch, E.论文数: 0 引用数: 0 h-index: 0机构: Hopitaux Univ Strasbourg, Serv Neurol, Strasbourg, France Serv Genet Moleculaire & Clin, Lyon, FranceRyvlin, P.论文数: 0 引用数: 0 h-index: 0机构: IDEE, Lyon, France Univ Lyon 1, Hosp Civils Lyon, Serv Epileptol, F-69365 Lyon, France Serv Genet Moleculaire & Clin, Lyon, FranceCalender, A.论文数: 0 引用数: 0 h-index: 0机构: Univ Lyon 1, Hosps Civils Lyon, Serv Genet, F-69365 Lyon, France Serv Genet Moleculaire & Clin, Lyon, FranceGenton, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Aix Marseille 2, Inst Neurobiol Mediterranee, INMED, INSERM,UMR901, Marseille, France Ctr St Paul, Marseille, France Serv Genet Moleculaire & Clin, Lyon, France
- [6] Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease[J]. EPILEPSIA, 2010, 51 (09) : 1691 - 1698Lesca, Gaetan论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet, Lyon, France Univ Lyon 1, F-69365 Lyon, France Inst Epilepsies Enfant & Adolescent IDEE, Lyon, France Hosp Civils Lyon, Serv Genet, Lyon, FranceBoutry-Kryza, Nadia论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet, Lyon, France Univ Lyon 1, F-69365 Lyon, France Hosp Civils Lyon, Serv Genet, Lyon, Francede Toffol, Bertrand论文数: 0 引用数: 0 h-index: 0机构: CHU Bretonneau, Serv Neurol, F-37044 Tours, France Hosp Civils Lyon, Serv Genet, Lyon, FranceMilh, Mathieu论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants La Timone, Serv Neurol Pediat, Marseille, France Hosp Civils Lyon, Serv Genet, Lyon, FranceSteschenko, Dominique论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Hop Enfants, Vandoeuvre Les Nancy, France Hosp Civils Lyon, Serv Genet, Lyon, FranceLemesle-Martin, Martine论文数: 0 引用数: 0 h-index: 0机构: Hop Gen, Lab Explorat Syst Nerveux, Dijon, France Hosp Civils Lyon, Serv Genet, Lyon, FranceMaillard, Louis论文数: 0 引用数: 0 h-index: 0机构: Univ Nancy, Serv Neurol, Hop Cent, Nancy, France Univ Nancy, CNRS, Ctr Rech Automat Nancy, UMR 7039, Nancy, France Hosp Civils Lyon, Serv Genet, Lyon, FranceFoletti, Giovanni论文数: 0 引用数: 0 h-index: 0机构: Inst Lavigny, Dept Neurol, Lavigny, Switzerland Hosp Civils Lyon, Serv Genet, Lyon, FranceRudolf, Gabrielle论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Serv Neurol, Strasbourg, France Hosp Civils Lyon, Serv Genet, Lyon, FranceNielsen, Jorgen Erik论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Neurogenet Sect, Inst Cellular & Mol Med, Copenhagen, Denmark Rigshosp, Copenhagen Univ Hosp, Dept Neurol, DK-2100 Copenhagen, Denmark Hosp Civils Lyon, Serv Genet, Lyon, FranceRogvi-Hansen, Bjarke A.论文数: 0 引用数: 0 h-index: 0机构: Rigshosp, Copenhagen Univ Hosp, Dept Neurol, DK-2100 Copenhagen, Denmark Hosp Civils Lyon, Serv Genet, Lyon, FranceErdal, Jesper论文数: 0 引用数: 0 h-index: 0机构: Rigshosp, Copenhagen Univ Hosp, Dept Neurol, DK-2100 Copenhagen, Denmark Hosp Civils Lyon, Serv Genet, Lyon, FranceMancini, Josette论文数: 0 引用数: 0 h-index: 0机构: Hop Enfants La Timone, Serv Neurol Pediat, Marseille, France Hosp Civils Lyon, Serv Genet, Lyon, FranceThauvin-Robinet, Christel论文数: 0 引用数: 0 h-index: 0机构: CHU Dijon, Hop Enfant, Ctr Genet, Dijon, France EPS Charles Nicolle, Serv Neurol, Tunis, Tunisia Hosp Civils Lyon, Serv Genet, Lyon, FranceM'Rrabet, Amel论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Hop Femme MeRe Enfant, Serv Neuropediat, Lyon, France Hosp Civils Lyon, Serv Genet, Lyon, FranceVille, Dorothee论文数: 0 引用数: 0 h-index: 0机构: Univ Lyon 1, F-69365 Lyon, France Hosp Civils Lyon, Serv Epileptol, Lyon, France Hosp Civils Lyon, Serv Genet, Lyon, FranceSzepetowski, Pierre论文数: 0 引用数: 0 h-index: 0机构: Univ Aix Marseille 2, INSERM, Inst Neurobiol Mediterranee INMED, UMR901, Marseille, France Hosp Civils Lyon, Serv Genet, Lyon, FranceRaffo, Emmanuel论文数: 0 引用数: 0 h-index: 0机构: CHU Nancy, Hop Enfants, Vandoeuvre Les Nancy, France Hosp Civils Lyon, Serv Genet, Lyon, FranceHirsch, Edouard论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Strasbourg, Serv Neurol, Strasbourg, France Hosp Civils Lyon, Serv Genet, Lyon, FranceRyvlin, Philippe论文数: 0 引用数: 0 h-index: 0机构: Univ Lyon 1, F-69365 Lyon, France Inst Epilepsies Enfant & Adolescent IDEE, Lyon, France Hosp Civils Lyon, Serv Epileptol, Lyon, France Hosp Civils Lyon, Serv Genet, Lyon, FranceCalender, Alain论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet, Lyon, France Univ Lyon 1, F-69365 Lyon, France Hosp Civils Lyon, Serv Genet, Lyon, FranceGenton, Pierre论文数: 0 引用数: 0 h-index: 0机构: Univ Aix Marseille 2, INSERM, Inst Neurobiol Mediterranee INMED, UMR901, Marseille, France Ctr St Paul, Marseille, France Hosp Civils Lyon, Serv Genet, Lyon, France
- [7] NHLRC1 repeat expansion in two beagles with Lafora disease[J]. JOURNAL OF SMALL ANIMAL PRACTICE, 2016, 57 (11) : 650 - 652Hajek, I.论文数: 0 引用数: 0 h-index: 0机构: Small Anim Referral Ctr Sibra, Bratislava 84101, Slovakia Small Anim Referral Ctr Sibra, Bratislava 84101, SlovakiaKettner, F.论文数: 0 引用数: 0 h-index: 0机构: Tygerberg Anim Hosp, ZA-7550 Cape Town, South Africa Small Anim Referral Ctr Sibra, Bratislava 84101, SlovakiaSimerdova, V.论文数: 0 引用数: 0 h-index: 0机构: Small Anim Referral Ctr Sibra, Bratislava 84101, Slovakia Univ Vet & Pharmaceut Sci Brno, Fac Vet Hyg & Ecol, Dept Anim Nutr, Brno 61242, Czech Republic Small Anim Referral Ctr Sibra, Bratislava 84101, SlovakiaRusbridge, C.论文数: 0 引用数: 0 h-index: 0机构: Fitzpatrick Referrals, Godalming GU7 2QQ, Surrey, England Univ Surrey, Sch Vet Med, Fac Hlth & Med Sci, Guildford GU2 7TE, Surrey, England Small Anim Referral Ctr Sibra, Bratislava 84101, SlovakiaWang, P.论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Hosp Sick Children, Program Genet & Genome Biol, Toronto, ON M5G 1X8, Canada Small Anim Referral Ctr Sibra, Bratislava 84101, SlovakiaMinassian, B. A.论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Dept Paediat, Fac Med, Toronto, ON M5S, Canada Small Anim Referral Ctr Sibra, Bratislava 84101, SlovakiaPalus, V.论文数: 0 引用数: 0 h-index: 0机构: Vet Clin ELPA, Trencin 91105, Slovakia Small Anim Referral Ctr Sibra, Bratislava 84101, Slovakia
- [8] The rare rs769301934 variant in NHLRC1 is a common cause of Lafora disease in Turkey[J]. Journal of Human Genetics, 2021, 66 : 1145 - 1151Garen Haryanyan论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsOzkan Ozdemir论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsKemal Tutkavul论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsAysin Dervent论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsSemih Ayta论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsCigdem Ozkara论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsBaris Salman论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsEmrah Yucesan论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsYesim Kesim论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsSeda Susgun论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsUgur Ozbek论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsBetul Baykan论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsSibel A. Ugur Iseri论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of GeneticsNerses Bebek论文数: 0 引用数: 0 h-index: 0机构: Aziz Sancar Institute of Experimental Medicine,Department of Genetics
- [9] A recurrent homozygous NHLRC1 variant in siblings with Lafora disease[J]. HUMAN GENOME VARIATION, 2018, 5Araya, Nami论文数: 0 引用数: 0 h-index: 0机构: NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanTakahashi, Yukitoshi论文数: 0 引用数: 0 h-index: 0机构: NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanShimono, Masayuki论文数: 0 引用数: 0 h-index: 0机构: Univ Occupat & Environm Hlth, Sch Med, Dept Pediat, Fukuoka, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanFukuda, Tomofumi论文数: 0 引用数: 0 h-index: 0机构: Univ Occupat & Environm Hlth, Sch Med, Dept Pediat, Fukuoka, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanKato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Showa Univ, Sch Med, Dept Pediat, Tokyo, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanNakashima, Mitsuko论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanMatsumoto, Naomichi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, JapanSaitsu, Hirotomo论文数: 0 引用数: 0 h-index: 0机构: Hamamatsu Univ Sch Med, Dept Biochem, Hamamatsu, Shizuoka, Japan NHO, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, Japan
- [10] Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease[J]. NEUROGENETICS, 2009, 10 (04) : 319 - 323Traore, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandLandoure, G.论文数: 0 引用数: 0 h-index: 0机构: UCL, Royal Free Hosp, London NW3 2PF, England Univ Bamako, Dept Neurosci, Bamako, Mali Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandMotley, W.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandSangare, M.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandMeilleur, K.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA NINR, NIH, Bethesda, MD 20892 USA Johns Hopkins Univ, Sch Nursing, Baltimore, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandCoulibaly, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandTraore, S.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandNiare, B.论文数: 0 引用数: 0 h-index: 0机构: Univ Bamako, Dept Neurosci, Bamako, Mali UCL, Royal Free Hosp, London NW3 2PF, EnglandMochel, F.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA Hop La Pitie Salpetriere, INSERM, U679, Paris, France UCL, Royal Free Hosp, London NW3 2PF, EnglandLa Pean, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandVortmeyer, A.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, EnglandMani, H.论文数: 0 引用数: 0 h-index: 0机构: NCI, NIH, Bethesda, MD 20892 USA UCL, Royal Free Hosp, London NW3 2PF, EnglandFischbeck, K. H.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Neurol Disorders & Stroke, NIH, Bethesda, MD USA UCL, Royal Free Hosp, London NW3 2PF, England