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- [1] Exome Sequencing Identifies GNB4 Mutations as a Cause of Dominant Intermediate Charcot-Marie-Tooth DiseaseAMERICAN JOURNAL OF HUMAN GENETICS, 2013, 92 (03) : 422 - 430论文数: 引用数: h-index:机构:Huang, Yen-Hua论文数: 0 引用数: 0 h-index: 0机构: Natl Yang Ming Univ, Dept Biochem, Sch Med, Taipei 11221, Taiwan Natl Yang Ming Univ, Ctr Syst & Synthet Biol, Taipei 11221, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanTsai, Pei-Chien论文数: 0 引用数: 0 h-index: 0机构: Natl Yang Ming Univ, Brain Res Ctr, Taipei 11221, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, Taiwan论文数: 引用数: h-index:机构:Pan, Hung-Chuan论文数: 0 引用数: 0 h-index: 0机构: Natl Yang Ming Univ, Fac Med, Taipei 11221, Taiwan Taichung Vet Gen Hosp, Dept Neurosurg, Taichung 40705, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanLu, Yi-Chun论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanChien, Hsin-Ju论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanLiu, Tze-Tze论文数: 0 引用数: 0 h-index: 0机构: Natl Yang Ming Univ, Genome Res Ctr, Taipei 11221, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanChang, Ming-Hong论文数: 0 引用数: 0 h-index: 0机构: Natl Yang Ming Univ, Dept Neurol, Sch Med, Taipei 11221, Taiwan Taichung Vet Gen Hosp, Sect Neurol, Taichung 40705, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanLin, Kon-Ping论文数: 0 引用数: 0 h-index: 0机构: Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, Taiwan Natl Yang Ming Univ, Dept Neurol, Sch Med, Taipei 11221, Taiwan Natl Yang Ming Univ, Brain Res Ctr, Taipei 11221, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, TaiwanTu, Pang-Hsien论文数: 0 引用数: 0 h-index: 0机构: Acad Sinica, Inst Biomed Sci, Taipei 11529, Taiwan Taipei Vet Gen Hosp, Dept Neurol, Taipei 11217, Taiwan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [2] Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GNB4 MutationsLIFE-BASEL, 2021, 11 (06):Kwon, Hye Mi论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaKim, Hyun Su论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Samsung Med Ctr, Dept Radiol, Sch Med, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaKim, Sang Beom论文数: 0 引用数: 0 h-index: 0机构: Kyung Hee Univ, Kyung Hee Univ Hosp Gangdong, Dept Neurol, Coll Med, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaPark, Jae Hong论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaNam, Da Eun论文数: 0 引用数: 0 h-index: 0机构: Kongju Natl Univ, Dept Biol Sci, Gongju 32588, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaLee, Ah Jin论文数: 0 引用数: 0 h-index: 0机构: Kongju Natl Univ, Dept Biol Sci, Gongju 32588, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaNam, Soo Hyun论文数: 0 引用数: 0 h-index: 0机构: Samsung Med Ctr, Inst Stem Cell & Regenerat Med, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South KoreaHwang, Soohyun论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Samsung Med Ctr, Dept Pathol & Translat Med, Sch Med, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South Korea论文数: 引用数: h-index:机构:Choi, Byung-Ok论文数: 0 引用数: 0 h-index: 0机构: Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South Korea Samsung Med Ctr, Inst Stem Cell & Regenerat Med, Seoul 06351, South Korea Sungkyunkwan Univ, Dept Hlth Sci & Technol, SAIHST, Seoul 06351, South Korea Sungkyunkwan Univ, Samsung Med Ctr, Dept Neurol, Sch Med, Seoul 06351, South Korea
- [3] A report of a family of intermediate Charcot-Marie-Tooth disease with concomitant mutations in the GNB4 and DNM2 genesEUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 322 - 322Burnyte, B.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, Lithuania Vilnius Univ Hosp, Santaros Klin, Ctr Med Genet, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, LithuaniaMorkuniene, A.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, Lithuania Vilnius Univ Hosp, Santaros Klin, Ctr Med Genet, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, LithuaniaAmbrozaityte, L.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, Lithuania Vilnius Univ Hosp, Santaros Klin, Ctr Med Genet, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, LithuaniaRegelskyte, V.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Fac Med, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, LithuaniaVaitkevicius, A.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Inst Clin Med, Fac Med, Vilnius, Lithuania Vilnius Univ Hosp, Santaros Klin, Ctr Neurol, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, LithuaniaKucinskas, V.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, LithuaniaUtkus, A.论文数: 0 引用数: 0 h-index: 0机构: Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, Lithuania Vilnius Univ Hosp, Santaros Klin, Ctr Med Genet, Vilnius, Lithuania Vilnius Univ, Inst Biomed Sci, Fac Med, Vilnius, Lithuania
- [4] Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseNEUROLOGY, 2005, 64 (10) : 1826 - 1826Zuchner, S论文数: 0 引用数: 0 h-index: 0Noureddine, M论文数: 0 引用数: 0 h-index: 0Kennerson, M论文数: 0 引用数: 0 h-index: 0Verhoeven, K论文数: 0 引用数: 0 h-index: 0Claeys, K论文数: 0 引用数: 0 h-index: 0De Jonghe, P论文数: 0 引用数: 0 h-index: 0Merory, J论文数: 0 引用数: 0 h-index: 0Oliveira, SA论文数: 0 引用数: 0 h-index: 0Speer, MC论文数: 0 引用数: 0 h-index: 0Stenger, JE论文数: 0 引用数: 0 h-index: 0Walizada, G论文数: 0 引用数: 0 h-index: 0Zhu, DQ论文数: 0 引用数: 0 h-index: 0Pericak-Vance, MA论文数: 0 引用数: 0 h-index: 0Nicholson, G论文数: 0 引用数: 0 h-index: 0Trimmerman, V论文数: 0 引用数: 0 h-index: 0Vance, JM论文数: 0 引用数: 0 h-index: 0
- [5] Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseNature Genetics, 2005, 37 : 289 - 294Stephan Züchner论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyMaher Noureddine论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyMarina Kennerson论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyKristien Verhoeven论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyKristl Claeys论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyPeter De Jonghe论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyJohn Merory论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologySofia A Oliveira论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyMarcy C Speer论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyJudith E Stenger论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyGina Walizada论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyDanqing Zhu论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyMargaret A Pericak-Vance论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyGarth Nicholson论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyVincent Timmerman论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of NeuropathologyJeffery M Vance论文数: 0 引用数: 0 h-index: 0机构: Center for Human Genetics,Department of Neuropathology
- [6] Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseNATURE GENETICS, 2005, 37 (03) : 289 - 294Züchner, S论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USA Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USANoureddine, M论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAKennerson, M论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAVerhoeven, K论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAClaeys, K论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USADe Jonghe, P论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAMerory, J论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAOliveira, SA论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USASpeer, MC论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAStenger, JE论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAWalizada, G论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAZhu, DQ论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAPericak-Vance, MA论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USANicholson, G论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USATimmerman, V论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USAVance, JM论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Dept Human Genet, Durham, NC 27710 USA
- [7] Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseJOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2005, 10 : 108 - 108Züchner, S论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USANoureddine, M论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAKennerson, M论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAVerhoeven, K论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAClaeys, K论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USADe Jonghe, P论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAMerory, J论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAOliveira, SA论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USASpeer, MC论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAStenger, JE论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAWalizada, G论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAZhu, D论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAPericak-Vance, MA论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USANicholson, GA论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USATimmerman, V论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USAVance, JM论文数: 0 引用数: 0 h-index: 0机构: Duke Univ, Med Ctr, Ctr Human Genet, B-2020 Durham, NC USA
- [8] Dominant mutations in ITPR3 cause Charcot-Marie-Tooth diseaseANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2020, 7 (10): : 1962 - 1972Ronkko, Julius论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandMolchanova, Svetlana论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland Univ Helsinki, Fac Bio & Environm Sci, Mol & Integrat Biosci Res Program, Helsinki, Finland Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandRevah-Politi, Anya论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Inst Genom Med, New York, NY USA Columbia Univ, Irving Med Ctr, Precis Genom Lab, New York, NY USA Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandPereira, Elaine M.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, Irving Med Ctr, New York, NY 10027 USA Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland论文数: 引用数: h-index:机构:Toppila, Jussi论文数: 0 引用数: 0 h-index: 0机构: Helsinki Univ Cent Hosp, Dept Clin Neurophysiol, Med Imaging Ctr, Helsinki, Finland Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland论文数: 引用数: h-index:机构:Ludwig, Anastasia论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Helsinki Inst Life Sci, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandNeumann, Julika论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Dept Microbiol & Immunol, Lab Adapt Immun, Leuven, Belgium VIB KU Leuven Ctr Brain & Dis Res, Leuven, Belgium Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandBultynck, Geert论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Lab Mol & Cellular Signaling, Dept Cellular & Mol Med, Leuven, Belgium Katholieke Univ Leuven, Leuven Kanker Inst, Leuven, Belgium Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandHumblet-Baron, Stephanie论文数: 0 引用数: 0 h-index: 0机构: VIB KU Leuven Ctr Brain & Dis Res, Leuven, Belgium Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland论文数: 引用数: h-index:机构:Paetau, Anders论文数: 0 引用数: 0 h-index: 0机构: HUSLAB, Dept Pathol, Helsinki, Finland Univ Helsinki, Helsinki, Finland Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandRivera, Claudio论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Helsinki Inst Life Sci, Neurosci Ctr, Helsinki, Finland Inst Neurobiol Mediterranee INMED UMR901, Marseille, France Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandHarms, Matthew B.论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Neurol, New York, NY USA Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, FinlandTyynismaa, Henna论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland Univ Helsinki, Helsinki Inst Life Sci, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Dept Med & Clin Genet, Helsinki, Finland Univ Helsinki, Stem Cells & Metab Res Program, Fac Med, Helsinki, Finland论文数: 引用数: h-index:机构:
- [9] Dominant mutations in ITPR3 cause Charcot-Marie-Tooth diseaseNEUROMUSCULAR DISORDERS, 2020, 30 : S167 - S168Ronkko, Julius论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandMolchanova, Svetlana论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland Univ Helsinki, Fac Bio & Environm Sci, Mol & Integrat Biosci Res Program, Helsinki, Finland Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandRevah-Politi, Anya论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Med Ctr, Inst Genom Med, New York, NY USA Columbia Univ, Irving Med Ctr, Precis Genom Lab, New York, NY USA Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandPereira, Elaine论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Pediat, Irving Med Ctr, New York, NY 10027 USA Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland论文数: 引用数: h-index:机构:Toppila, Jussi论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Cent Hosp, Med Imaging Ctr, Dept Clin Neurophysiol, Helsinki, Finland Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland论文数: 引用数: h-index:机构:Ludwig, Anastasia论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Helsinki Inst Life Sci, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandNeumann, Julika论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Lab Adapt Immun, Dept Microbiol & Immunol, Leuven, Belgium VIB KU Leuven, Ctr Brain & Dis Res, Leuven, Belgium Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandHumblet-Baron, Stephanie论文数: 0 引用数: 0 h-index: 0机构: VIB KU Leuven, Ctr Brain & Dis Res, Leuven, Belgium Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandBultynck, Geert论文数: 0 引用数: 0 h-index: 0机构: Katholieke Univ Leuven, Lab Mol & Cellular Signaling, Dept Cellular & Mol Med, Leuven, Belgium Leuven Kanker Inst, Leuven, Belgium Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland论文数: 引用数: h-index:机构:Patau, Anders论文数: 0 引用数: 0 h-index: 0机构: HUSLAB, Dept Pathol, Helsinki, Finland Univ Helsinki, Helsinki, Finland Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandRivera, Claudio论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Helsinki Inst Life Sci, Neurosci Ctr, Helsinki, Finland Inst Neurobiol Mediterranee INMED, UMR901, Marseille, France Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandHarms, Matthew论文数: 0 引用数: 0 h-index: 0机构: Columbia Univ, Dept Neurol, New York, NY USA Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, FinlandTyynismaa, Henna论文数: 0 引用数: 0 h-index: 0机构: Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland Univ Helsinki, Helsinki Inst Life Sci, Neurosci Ctr, Helsinki, Finland Univ Helsinki, Dept Med & Clin Genet, Helsinki, Finland Univ Helsinki, Fac Med, Stem Cells & Metab Res Program, Helsinki, Finland论文数: 引用数: h-index:机构:
- [10] Molecular mechanisms of dynamin 2 mutations in dominant intermediate Charcot-Marie-Tooth diseaseNEUROLOGY, 2007, 68 (12) : A341 - A341Wang, Gaofeng论文数: 0 引用数: 0 h-index: 0Kennerson, Marina论文数: 0 引用数: 0 h-index: 0Biscocho, Dhani论文数: 0 引用数: 0 h-index: 0Noureddine, Maher论文数: 0 引用数: 0 h-index: 0Myers, Simon论文数: 0 引用数: 0 h-index: 0Nicholson, Garth论文数: 0 引用数: 0 h-index: 0Vance, Jeffery M.论文数: 0 引用数: 0 h-index: 0Zuechner, Stephan论文数: 0 引用数: 0 h-index: 0