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- [21] A homozygous variant in RRM2B is associated with severe metabolic acidosis and early neonatal deathEUROPEAN JOURNAL OF MEDICAL GENETICS, 2019, 62 (11)Penque, Brent A.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USASu, Leila论文数: 0 引用数: 0 h-index: 0机构: Taipei Med Univ, Coll Med Technol, Dept Canc Biol & Drug Discovery, 250 Wu Hsing St, Taipei 110, Taiwan Sinoamer Canc Fdn, Temple City, CA USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USAWang, Jianghai论文数: 0 引用数: 0 h-index: 0机构: Taipei Med Univ, Coll Med Technol, Dept Canc Biol & Drug Discovery, 250 Wu Hsing St, Taipei 110, Taiwan Sinoamer Canc Fdn, Temple City, CA USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USAJi, Weizhen论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USABale, Allen论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USALuh, Frank论文数: 0 引用数: 0 h-index: 0机构: Taipei Med Univ, Coll Med Technol, Dept Canc Biol & Drug Discovery, 250 Wu Hsing St, Taipei 110, Taiwan Sinoamer Canc Fdn, Temple City, CA USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USAFulbright, Robert K.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Dept Radiol & Biomed Imaging, Sch Med, New Haven, CT USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USASarmast, Uzair论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Dept Radiol & Biomed Imaging, Sch Med, New Haven, CT USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USASega, Annalisa G.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USAKonstantino, Monica论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USASpencer-Manzon, Michele论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA论文数: 引用数: h-index:机构:Yen, Yun论文数: 0 引用数: 0 h-index: 0机构: Taipei Med Univ, Coll Med Technol, Dept Canc Biol & Drug Discovery, 250 Wu Hsing St, Taipei 110, Taiwan Sinoamer Canc Fdn, Temple City, CA USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USALakhani, Saquib A.论文数: 0 引用数: 0 h-index: 0机构: Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA Yale Univ, Sch Med, Sect Crit Care Med, Pediat Genom Discovery Program,Dept Pediat, New Haven, CT 06520 USA
- [22] Clinical spectrum of SCN2A mutations expanding to Ohtahara syndromeNEUROLOGY, 2013, 81 (11) : 992 - 998论文数: 引用数: h-index:机构:Kato, Mitsuhiro论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Fac Med, Dept Pediat, Yamagata 990, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanOsaka, Hitoshi论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Div Neurol, Yokohama, Kanagawa, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanYamashita, Sumimasa论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Div Neurol, Yokohama, Kanagawa, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanNakagawa, Eiji论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Hosp, Natl Ctr Neurol & Psychiat, Dept Child Neurol, Tokyo, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanHaginoya, Kazuhiro论文数: 0 引用数: 0 h-index: 0机构: Takuto Rehabil Ctr Children, Dept Pediat Neurol, Sendai, Miyagi, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanTohyama, Jun论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Epilepsy Ctr, Dept Pediat, Niigata, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanOkuda, Mitsuko论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Div Neurol, Yokohama, Kanagawa, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanWada, Takahito论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Clin Res Inst, Div Neurol, Yokohama, Kanagawa, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanShimakawa, Shuichi论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Coll Hosp, Dept Pediat, Osaka, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanImai, Katsumi论文数: 0 引用数: 0 h-index: 0机构: Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanTakeshita, Saoko论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Med Ctr, Dept Pediat, Yokohama, Kanagawa 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanIshiwata, Hisako论文数: 0 引用数: 0 h-index: 0机构: Tokyo Metropolitan Bokuto Gen Hosp, Dept Pediat, Tokyo, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanLev, Dorit论文数: 0 引用数: 0 h-index: 0机构: Wolfson Med Ctr, Metab Neurogenet Clin, Holon, Israel Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanLerman-Sagie, Tally论文数: 0 引用数: 0 h-index: 0机构: Wolfson Med Ctr, Metab Neurogenet Clin, Holon, Israel Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanCervantes-Barragan, David E.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Pediat, Dept Human Genet, Mexico City, DF, Mexico Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanVillarroel, Camilo E.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Pediat, Dept Human Genet, Mexico City, DF, Mexico Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanOhfu, Masaharu论文数: 0 引用数: 0 h-index: 0机构: Okinawa Nanbu Med Ctr, Div Child Neurol, Okinawa, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanWritzl, Karin论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Ljubljana, Inst Med Genet, Ljubljana, Slovenia Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanStrazisar, Barbara Gnidovec论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Dept Child Adolescent & Dev Neurol, Ljubljana, Slovenia Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanHirabayashi, Shinichi论文数: 0 引用数: 0 h-index: 0机构: Nagano Childrens Hosp, Dept Neurol, Nagano, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan论文数: 引用数: h-index:机构:Reid, Diane Myles论文数: 0 引用数: 0 h-index: 0机构: Univ Toronto, Hosp Sick Children, Div Clin & Metab Genet, Toronto, ON M5S 1A1, Canada Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanNishiyama, Kiyomi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanKodera, Hirofumi论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, 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 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanTsurusaki, Yoshinori论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanMiyake, Noriko论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, JapanHayasaka, Kiyoshi论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Fac Med, Dept Pediat, Yamagata 990, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, 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 232, Japan Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan论文数: 引用数: h-index:机构:
- [23] CLINICAL SPECTRUM OF SCN2A MUTATIONS EXPANDING TO OHTAHARA SYNDROMEEPILEPSIA, 2013, 54 : 193 - 193论文数: 引用数: h-index:机构:Kato, M.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Dept Pediat, Yamagata 990, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanOsaka, H.论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Neurol, Yokohama, Kanagawa, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanYamashita, S.论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Neurol, Yokohama, Kanagawa, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanNakagawa, E.论文数: 0 引用数: 0 h-index: 0机构: Natl Ctr Hosp, Natl Ctr Neurol & Psychiat, Tokyo, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanHaginoya, K.论文数: 0 引用数: 0 h-index: 0机构: Takuto Rehabil Ctr Children, Sendai, Miyagi, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanTohyama, J.论文数: 0 引用数: 0 h-index: 0机构: Nishi Niigata Chuo Natl Hosp, Epilepsy Ctr, Niigata, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanOkuda, M.论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Neurol, Yokohama, Kanagawa, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanWada, T.论文数: 0 引用数: 0 h-index: 0机构: Kanagawa Childrens Med Ctr, Div Neurol, Yokohama, Kanagawa, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanShimakawa, S.论文数: 0 引用数: 0 h-index: 0机构: Osaka Med Coll Hosp, Osaka, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanImai, K.论文数: 0 引用数: 0 h-index: 0机构: Natl Epilepsy Ctr, Shizuoka Inst Epilepsy & Neurol Disorders, Shizuoka, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanTakeshita, S.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Med Ctr, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanIshiwata, H.论文数: 0 引用数: 0 h-index: 0机构: Tokyo Metropolitan Bokuto Gen Hosp, Tokyo, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanLev, D.论文数: 0 引用数: 0 h-index: 0机构: Wolfson Med Ctr, Metab Neurogenet Clin, Holon, Israel Yamagata Univ, Dept Pediat, Yamagata 990, JapanLerman-Sagie, T.论文数: 0 引用数: 0 h-index: 0机构: Wolfson Med Ctr, Metab Neurogenet Clin, Holon, Israel Yamagata Univ, Dept Pediat, Yamagata 990, JapanCervantes-Barragan, D. E.论文数: 0 引用数: 0 h-index: 0机构: Natl Inst Pediat, Dept Human Genet, Mexico City, DF, Mexico Yamagata Univ, Dept Pediat, Yamagata 990, JapanVillarroel, C. E.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Dept Pediat, Yamagata 990, JapanOhfu, M.论文数: 0 引用数: 0 h-index: 0机构: Okinawa Nanbu Med Ctr, Okinawa, Japan Childrens Med Ctr, Okinawa, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanWritzl, K.论文数: 0 引用数: 0 h-index: 0机构: Univ Med Ctr Ljubljana, Inst Med Genet, Ljubljana, Slovenia Yamagata Univ, Dept Pediat, Yamagata 990, JapanStrazisar, B. G.论文数: 0 引用数: 0 h-index: 0机构: Univ Childrens Hosp, Dept Child Adolescent & Dev Neurol, Ljubljana, Slovenia Yamagata Univ, Dept Pediat, Yamagata 990, JapanHirabayashi, S.论文数: 0 引用数: 0 h-index: 0机构: Nagano Childrens Hosp, Nagano, Japan Yamagata Univ, Dept Pediat, Yamagata 990, Japan论文数: 引用数: h-index:机构:Reid, Myles D.论文数: 0 引用数: 0 h-index: 0机构: Hosp Sick Children, Div Clin & Metab Genet, Toronto, ON M5G 1X8, Canada Yamagata Univ, Dept Pediat, Yamagata 990, JapanNishiyama, K.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanKodera, H.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanNakashima, M.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanTsurusaki, Y.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanMiyake, N.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanHayasaka, K.论文数: 0 引用数: 0 h-index: 0机构: Yamagata Univ, Dept Pediat, Yamagata 990, Japan Yamagata Univ, Dept Pediat, Yamagata 990, JapanMatsumoto, N.论文数: 0 引用数: 0 h-index: 0机构: Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 232, Japan Yamagata Univ, Dept Pediat, Yamagata 990, Japan论文数: 引用数: h-index:机构:
- [24] Diagnosing mitochondrial, neurogastrointestinal leukoencephalopathy requires mutations in TYMP1, POLG1, LIG1, or RRM2BJournal of Medical Case Reports, 17Josef Finsterer论文数: 0 引用数: 0 h-index: 0机构: Neurology and Neurophysiology Center,
- [25] Two novel RRM2B gene mutations in a patient with autosomal recessive progressive external ophthalmoplegia, encephalopathy and cytochrome c oxidase deficiencyMITOCHONDRION, 2012, 12 (05) : 562 - 563Bai, Renkui论文数: 0 引用数: 0 h-index: 0机构: GeneDx Inc, Gaithersburg, MD 20877 USA Childrens Hosp Cent Calif, Dept Med Genet, Madera, CA 93704 USAHauser, Natalie S.论文数: 0 引用数: 0 h-index: 0机构: Childrens Hosp Cent Calif, Dept Med Genet, Madera, CA 93704 USA Childrens Hosp Cent Calif, Dept Med Genet, Madera, CA 93704 USABai, Renkui论文数: 0 引用数: 0 h-index: 0机构: GeneDx Inc, Gaithersburg, MD 20877 USA Childrens Hosp Cent Calif, Dept Med Genet, Madera, CA 93704 USA
- [26] A novel RRM2B gene variant associated with Telbivudine-induced mitochondrial myopathyJOURNAL OF THE NEUROLOGICAL SCIENCES, 2015, 358 (1-2) : 481 - 483Hernandez-Lain, Aurelio论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainGuerrero, Antonio Mendez论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Dept Neurol, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainDominguez-Gonzalez, Cristina论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Dept Neurol, Neuromuscular Unit, Madrid 28041, Spain CIBERER, U723, Madrid, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainFernandez-Vazquez, Inmaculada论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Dept Gastroenterol & Hepatol, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainGata Maya, David论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Dept Neurol, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainDelmiro, Aitor论文数: 0 引用数: 0 h-index: 0机构: CIBERER, U723, Madrid, Spain Hosp Univ 12 Octubre, Res Inst, Mitochondrial Dis Lab, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainArenas, Joaquin论文数: 0 引用数: 0 h-index: 0机构: CIBERER, U723, Madrid, Spain Hosp Univ 12 Octubre, Res Inst, Mitochondrial Dis Lab, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainRuiz Morales, Juan论文数: 0 引用数: 0 h-index: 0机构: Hosp Univ 12 Octubre, Dept Neurol, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainBlazquez, Alberto论文数: 0 引用数: 0 h-index: 0机构: CIBERER, U723, Madrid, Spain Hosp Univ 12 Octubre, Res Inst, Mitochondrial Dis Lab, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainMoran, Maria论文数: 0 引用数: 0 h-index: 0机构: CIBERER, U723, Madrid, Spain Hosp Univ 12 Octubre, Res Inst, Mitochondrial Dis Lab, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, SpainMartin, Miguel A.论文数: 0 引用数: 0 h-index: 0机构: CIBERER, U723, Madrid, Spain Hosp Univ 12 Octubre, Res Inst, Mitochondrial Dis Lab, Madrid 28041, Spain Hosp Univ 12 Octubre, Madrid Res Inst, Dept Pathol Neuropathol, Madrid 28041, Spain
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- [28] Gene aberrations of RRM1 and RRM2B and outcome of advanced breast cancer after treatment with docetaxel with or without gemcitabineBMC CANCER, 2013, 13Jorgensen, Charlotte L. T.论文数: 0 引用数: 0 h-index: 0机构: Herlev Univ Hosp, Dept Pathol, Copenhagen, Denmark Herlev Univ Hosp, Dept Pathol, Copenhagen, DenmarkEjlertsen, Bent论文数: 0 引用数: 0 h-index: 0机构: Rigshosp, Danish Breast Canc Cooperat Grp DBCG Registry, DK-2100 Copenhagen, Denmark Herlev Univ Hosp, Dept Pathol, Copenhagen, DenmarkBjerre, Karsten D.论文数: 0 引用数: 0 h-index: 0机构: Rigshosp, Danish Breast Canc Cooperat Grp DBCG Registry, DK-2100 Copenhagen, Denmark Herlev Univ Hosp, Dept Pathol, Copenhagen, DenmarkBalslev, Eva论文数: 0 引用数: 0 h-index: 0机构: Herlev Univ Hosp, Dept Pathol, Copenhagen, Denmark Herlev Univ Hosp, Dept Pathol, Copenhagen, DenmarkNielsen, Dorte L.论文数: 0 引用数: 0 h-index: 0机构: Herlev Univ Hosp, Dept Oncol, Copenhagen, Denmark Herlev Univ Hosp, Dept Pathol, Copenhagen, DenmarkNielsen, Kirsten V.论文数: 0 引用数: 0 h-index: 0机构: Capital Reg Denmark, VIF, Ctr Innovat & Res, Copenhagen, Denmark Herlev Univ Hosp, Dept Pathol, Copenhagen, Denmark
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