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A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.
Hong, Young Bin; Joo, Jaesoon; Hyun, Young Se; Kwak, Geon; Choi, Yu-Ri; Yeo, Ha Kyung; Jwa, Dong Hwan; Kim, Eun Ja; Mo, Won Min; Nam, Soo Hyun; Kim, Sung Min; Yoo, Jeong Hyun; Koo, Heasoo; Park, Hwan Tae; Chung, Ki Wha; Choi, Byung-Ok.
Afiliação
  • Hong YB; Stem Cell and Regenerative Medicine Center, Samsung Medical Center, Seoul, Korea.
  • Joo J; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Science and Technology, Sungkyunkwan University, Seoul, Korea.
  • Hyun YS; Department of Biological Science, Kongju National University, Gongju, Korea.
  • Kwak G; Department of Health Sciences and Technology, Samsung Advanced Institute for Health Science and Technology, Sungkyunkwan University, Seoul, Korea.
  • Choi YR; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Yeo HK; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Jwa DH; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Kim EJ; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Mo WM; Neuroscience Center, Samsung Medical Center, Seoul, Korea.
  • Nam SH; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Kim SM; Department of Biological Science, Kongju National University, Gongju, Korea.
  • Yoo JH; Department of Biological Science, Kongju National University, Gongju, Korea.
  • Koo H; Department of Radiology, Ewha Womans University, School of Medicine, Seoul, Korea.
  • Park HT; Department of Pathology, Ewha Womans University, School of Medicine, Seoul, Korea.
  • Chung KW; Department of Physiology, College of Medicine, Dong-A University, Busan, Korea.
  • Choi BO; Department of Biological Science, Kongju National University, Gongju, Korea.
PLoS Genet ; 12(2): e1005829, 2016 Feb.
Article em En | MEDLINE | ID: mdl-26828946
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Doenças Desmielinizantes / Proteína P2 de Mielina / Genes Dominantes Tipo de estudo: Etiology_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
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PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Doenças Desmielinizantes / Proteína P2 de Mielina / Genes Dominantes Tipo de estudo: Etiology_studies Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article