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- [21] Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutationARCHIVES OF NEUROLOGY, 2006, 63 (12) : 1701 - 1706Jeppesen, Tina D.论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Natl Hosp, Rigshosp, Copenhagen Muscle Res Ctr, Copenhagen, DenmarkSchwartz, Marianne论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Natl Hosp, Rigshosp, Copenhagen Muscle Res Ctr, Copenhagen, DenmarkFrederiksen, Anja L.论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Natl Hosp, Rigshosp, Copenhagen Muscle Res Ctr, Copenhagen, DenmarkWibrand, Flemming论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Natl Hosp, Rigshosp, Copenhagen Muscle Res Ctr, Copenhagen, DenmarkOlsen, David B.论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Natl Hosp, Rigshosp, Copenhagen Muscle Res Ctr, Copenhagen, DenmarkVissing, John论文数: 0 引用数: 0 h-index: 0机构: Univ Copenhagen, Natl Hosp, Rigshosp, Copenhagen Muscle Res Ctr, Copenhagen, Denmark
- [22] A disease-associated G5703A mutation in the human mitochondrial DNA causes a conformational change and a marked disease in steady-state levels of the mitochondrial tRNAAsn.AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A310 - A310Hao, H论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Neurol, Miami, FL 33152 USA Univ Miami, Dept Neurol, Miami, FL 33152 USAMoraes, CT论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Dept Neurol, Miami, FL 33152 USA Univ Miami, Dept Neurol, Miami, FL 33152 USA
- [23] G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlationNEUROBIOLOGY OF AGING, 2022, 118 : 124 - 128Martinelli, Ilaria论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyZucchi, Elisabetta论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Biomed Metab & Neural Sci, Via Giuseppe Campi 287, I-41125 Modena, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyPensato, Viviana论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol Carlo Besta, Unit Med Genet & Neurogenet, Via Celoria 11, I-20133 Milan, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyGellera, Cinzia论文数: 0 引用数: 0 h-index: 0机构: Fdn IRCCS Ist Neurol Carlo Besta, Unit Med Genet & Neurogenet, Via Celoria 11, I-20133 Milan, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyTraynor, Bryan J.论文数: 0 引用数: 0 h-index: 0机构: NIA, Neuromuscular Dis Res Sect, Lab Neurogenet, NIH, Bethesda, MD USA Johns Hopkins Univ, Dept Neurol, Baltimore, MD 21218 USA UCL, Reta Lila Weston Inst, UCL Queen Sq Inst Neurol, London, England Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyGianferrari, Giulia论文数: 0 引用数: 0 h-index: 0机构: Univ Modena & Reggio Emilia, Dept Biomed Metab & Neural Sci, Via Giuseppe Campi 287, I-41125 Modena, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyChio, Adriano论文数: 0 引用数: 0 h-index: 0机构: Univ Torino, ALS Ctr Rita Levi Montalcini, Dept Neurosci, Turin, Italy Azienda Osped Univ Citta Salute & Sci, Turin, Italy Neurosci Inst Torino, Turin, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, ItalyMandrioli, Jessica论文数: 0 引用数: 0 h-index: 0机构: Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, Italy Univ Modena & Reggio Emilia, Dept Biomed Metab & Neural Sci, Via Giuseppe Campi 287, I-41125 Modena, Italy Azienda Osped Univ Modena, S Agostino Estense Hosp, Dept Neurosci, Neurol Unit, I-41126 Modena, Italy
- [24] Mutation Spectrum and Genotype-Phenotype Correlation in Cornelia de Lange SyndromeHUMAN MUTATION, 2013, 34 (12) : 1589 - 1596Mannini, Linda论文数: 0 引用数: 0 h-index: 0机构: CNR, Ist Ric Genet & Biomed, I-56100 Pisa, Italy CNR, Ist Ric Genet & Biomed, I-56100 Pisa, ItalyCucco, Francesco论文数: 0 引用数: 0 h-index: 0机构: CNR, Ist Ric Genet & Biomed, I-56100 Pisa, Italy Univ Pisa, Dipartimento Biol, Pisa, Italy CNR, Ist Ric Genet & Biomed, I-56100 Pisa, ItalyQuarantotti, Valentina论文数: 0 引用数: 0 h-index: 0机构: CNR, Ist Ric Genet & Biomed, I-56100 Pisa, Italy CNR, Ist Ric Genet & Biomed, I-56100 Pisa, ItalyKrantz, Ian D.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Philadelphia, Div Human Genet, Philadelphia, PA 19104 USA Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA CNR, Ist Ric Genet & Biomed, I-56100 Pisa, ItalyMusio, Antonio论文数: 0 引用数: 0 h-index: 0机构: CNR, Ist Ric Genet & Biomed, I-56100 Pisa, Italy CNR, Ist Ric Genet & Biomed, I-56100 Pisa, Italy
- [25] Cardiomyopathies due to mutations in the myopalladin gene: Genotype-phenotype correlationPROGRESS IN PEDIATRIC CARDIOLOGY, 2011, 31 (02) : 139 - +Purevjav, Enkhsaikhan论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAArimura, Takuro论文数: 0 引用数: 0 h-index: 0机构: Tokyo Med & Dent Univ, Med Res Inst, Dept Mol Pathogenesis, Tokyo, Japan Tokyo Med & Dent Univ, Sch Biomed Sci, Lab Genome Divers, Tokyo, Japan Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAAugustin, Sibylle论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Med Pediat & Mol Pharmacol, Rochester, MN USA Mayo Clin, Dept Expt Therapeut, Rochester, MN USA Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USANunoda, Shinichi论文数: 0 引用数: 0 h-index: 0机构: Tokyo Womens Med Univ, Dept Med, Tokyo, Japan Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAVarela, Jaquelin论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Pediat, Cardiol Sect, Houston, TX 77030 USA Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAKearney, Debra L.论文数: 0 引用数: 0 h-index: 0机构: Baylor Coll Med, Dept Pediat, Sect Pathol, Houston, TX 77030 USA Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAMcKenna, William论文数: 0 引用数: 0 h-index: 0机构: Heart Hosp, Dept Cardiol, London, England Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAAckerman, Michael J.论文数: 0 引用数: 0 h-index: 0机构: Mayo Clin, Dept Med Pediat & Mol Pharmacol, Rochester, MN USA Mayo Clin, Dept Expt Therapeut, Rochester, MN USA Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USAKimura, Akinori论文数: 0 引用数: 0 h-index: 0机构: Tokyo Med & Dent Univ, Med Res Inst, Dept Mol Pathogenesis, Tokyo, Japan Tokyo Med & Dent Univ, Sch Biomed Sci, Lab Genome Divers, Tokyo, Japan Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USATowbin, Jeffrey A.论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USA Cincinnati Childrens Hosp Med Ctr, Inst Heart, Cincinnati, OH 45229 USA
- [26] MUTATION SCREENING AND GENOTYPE-PHENOTYPE CORRELATION IN NF2 PATIENTSJOURNAL OF MEDICAL GENETICS, 1995, 32 (02) : 138 - 138BOURN, D论文数: 0 引用数: 0 h-index: 0机构: UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLANDMASON, S论文数: 0 引用数: 0 h-index: 0机构: UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLANDTEKES, S论文数: 0 引用数: 0 h-index: 0机构: UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLANDCARTER, SA论文数: 0 引用数: 0 h-index: 0机构: UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLANDEVANS, DGR论文数: 0 引用数: 0 h-index: 0机构: UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLANDSTRACHAN, T论文数: 0 引用数: 0 h-index: 0机构: UNIV NEWCASTLE UPON TYNE,DIV HUMAN GENET,NEWCASTLE TYNE NE1 7RU,TYNE & WEAR,ENGLAND
- [27] Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in TaiwanCLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2020, 48 (04): : 486 - 499Chen, Zhen-Ji论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaLin, Keng-Hung论文数: 0 引用数: 0 h-index: 0机构: Taichung Vet Gen Hosp, Dept Ophthalmol, Taichung, Taiwan Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaLee, Shi-Huang论文数: 0 引用数: 0 h-index: 0机构: Taichung Tzu Chi Hosp, Dept Ophthalmol, Taichung, Taiwan Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaShen, Ren-Juan论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaFeng, Zhuo-Kun论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaWang, Xiao-Fang论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaHuang, Xiu-Feng论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaHuang, Zhi-Qin论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R ChinaJin, Zi-Bing论文数: 0 引用数: 0 h-index: 0机构: Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China Wenzhou Med Univ, Inst Stem Cell Res, Lab Stem Cell & Retinal Regenerat, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Ctr Int Res Regenerat Med & Neurogenet, Wenzhou, Peoples R China Wenzhou Med Univ, Natl Clin Res Ctr Ocular Dis, State Key Lab Ophthalmol Optometry & Visual Sci, Wenzhou, Peoples R China Wenzhou Med Univ, Eye Hosp, Div Ophthalm Genet, Wenzhou 325027, Peoples R China
- [28] Mutation screening and genotype-phenotype correlation in 32 families with Wilson diseaseJOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE, 1999, 12 (04): : 321 - 329Bost, M论文数: 0 引用数: 0 h-index: 0机构: UNESCO, Trace Element Inst, F-69342 Lyon 07, FranceLachaux, A论文数: 0 引用数: 0 h-index: 0机构: UNESCO, Trace Element Inst, F-69342 Lyon 07, FranceAccominotti, M论文数: 0 引用数: 0 h-index: 0机构: UNESCO, Trace Element Inst, F-69342 Lyon 07, FranceVandenberghe, A论文数: 0 引用数: 0 h-index: 0机构: UNESCO, Trace Element Inst, F-69342 Lyon 07, France
- [29] Distal hereditary motor neuropathies: Mutation spectrum and genotype-phenotype correlationEUROPEAN JOURNAL OF NEUROLOGY, 2021, 28 (04) : 1334 - 1343Frasquet, Marina论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, Spain Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainRojas-Garcia, Ricard论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Santa Creu & Sant Pau, Dept Neurol, Neuromuscular Dis Unit, Barcelona, Spain Univ Autonoma Barcelona, Barcelona, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainArgente-Escrig, Herminia论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainVazquez-Costa, Juan Francisco论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, Spain Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Univ Valencia, Dept Med, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainMuelas, Nuria论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, Spain Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainVilchez, Juan Jesus论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainSivera, Rafael论文数: 0 引用数: 0 h-index: 0机构: Hosp Francesc Borja, Dept Neurol, Gandia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainMillet, Elvira论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Dept Clin Neurophysiol, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainBarreiro, Marisa论文数: 0 引用数: 0 h-index: 0机构: Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainDiaz-Manera, Jordi论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Santa Creu & Sant Pau, Dept Neurol, Neuromuscular Dis Unit, Barcelona, Spain Univ Autonoma Barcelona, Barcelona, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainTuron-Sans, Janina论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Santa Creu & Sant Pau, Dept Neurol, Neuromuscular Dis Unit, Barcelona, Spain Univ Autonoma Barcelona, Barcelona, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainCortes-Vicente, Elena论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Santa Creu & Sant Pau, Dept Neurol, Neuromuscular Dis Unit, Barcelona, Spain Univ Autonoma Barcelona, Barcelona, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainQuerol, Luis论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Hosp Santa Creu & Sant Pau, Dept Neurol, Neuromuscular Dis Unit, Barcelona, Spain Univ Autonoma Barcelona, Barcelona, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainRamirez-Jimenez, Laura论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Principe Felipe CIPF, Dept Genom & Translat Genet, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainMartinez-Rubio, Dolores论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Principe Felipe CIPF, Unit Genet & Genom Neuromuscular & Neurodegenerat, Valencia, Spain INCLIVA & IIS La Fe CIPF, Rare Dis Joint Units, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainSanchez-Monteagudo, Ana论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Principe Felipe CIPF, Unit Genet & Genom Neuromuscular & Neurodegenerat, Valencia, Spain INCLIVA & IIS La Fe CIPF, Rare Dis Joint Units, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainEspinos, Carmen论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Principe Felipe CIPF, Unit Genet & Genom Neuromuscular & Neurodegenerat, Valencia, Spain INCLIVA & IIS La Fe CIPF, Rare Dis Joint Units, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainSevilla, Teresa论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, Spain Inst Invest Sanitaria La Fe, Neuromuscular & Ataxias Res Grp, Valencia, Spain Ctr Invest Biomed Red Enfermedades Raras CIBERER, Valencia, Spain Univ Valencia, Dept Med, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, SpainLupo, Vincenzo论文数: 0 引用数: 0 h-index: 0机构: Ctr Invest Principe Felipe CIPF, Unit Genet & Genom Neuromuscular & Neurodegenerat, Valencia, Spain INCLIVA & IIS La Fe CIPF, Rare Dis Joint Units, Valencia, Spain Hosp Univ & Politecn La Fe, Dept Neurol, Neuromuscular Dis Unit, Valencia, Spain
- [30] Genotype-Phenotype Correlation in a New Fabry-Disease-Causing MutationMEDICINA-LITHUANIA, 2019, 55 (05):Cerkauskaite, Agne论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, Lithuania Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, Lithuania论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Ding, Can论文数: 0 引用数: 0 h-index: 0机构: Johannes Gutenberg Univ Mainz, Univ Med Ctr, Inst Human Genet, Langenbeckstr 1, D-55131 Mainz, Germany Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, LithuaniaRolfs, Arndt论文数: 0 引用数: 0 h-index: 0机构: Univ Rostock, Gehlsheimerstr 20, D-18147 Rostock, Germany Centogene AG, Strande 7, D-18055 Rostock, Germany Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, LithuaniaVenceviciene, Lina论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Fac Med, Inst Clin Med, Santariskiu 2, LT-08406 Vilnius, Lithuania Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, LithuaniaBarysiene, Jurate论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Fac Med, Inst Clin Med, Santariskiu 2, LT-08406 Vilnius, Lithuania Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, LithuaniaKazenaite, Edita论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, Lithuania Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, LithuaniaSadauskiene, Egle论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Fac Med, Inst Clin Med, Santariskiu 2, LT-08406 Vilnius, Lithuania Vilnius Univ, Fac Med, Inst Biomed Sci, Santariskiu 2, LT-08406 Vilnius, Lithuania