Your browser doesn't support javascript.
loading
Loss-of-function of EBP50 is a new cause of hereditary peripheral neuropathy: EBP50 functions in peripheral nerve system.
Song, Gyun Jee; Gupta, Deepak Prasad; Rahman, Md Habibur; Park, Hwan Tae; Al Ghouleh, Imad; Bisello, Alessandro; Lee, Maan-Gee; Park, Jae-Yong; Park, Hyun Ho; Jun, Jin Hyun; Chung, Ki Wha; Choi, Byung-Ok; Suk, Kyoungho.
Afiliación
  • Song GJ; Department of Medical Science, Institute for Bio-Medical Convergence, Catholic Kwandong University, International St. Mary's Hospital, Incheon, Republic of Korea.
  • Gupta DP; Department of Pharmacology, Brain Science and Engineering Institute, BK21 Plus KNU Biomedical Convergence Program, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
  • Rahman MH; Department of Pharmacology, Brain Science and Engineering Institute, BK21 Plus KNU Biomedical Convergence Program, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
  • Park HT; Department of Molecular Neuroscience, College of Medicine, Dong-A University, Busan, Republic of Korea.
  • Al Ghouleh I; Division of Cardiology, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
  • Bisello A; Department of Pharmacology and Chemical Biology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.
  • Lee MG; Department of Pharmacology, Brain Science and Engineering Institute, BK21 Plus KNU Biomedical Convergence Program, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
  • Park JY; School of Biosystems and Biomedical Sciences, College of Health Sciences, Korea University, Seoul, Republic of Korea.
  • Park HH; College of Pharmacy, Chung-Ang University, Seoul, Republic of Korea.
  • Jun JH; Department of Senior Healthcare, BK21 Plus Program, Graduate School of Eulji University, Department of Biomedical Laboratory Science, College of Health Science, Eulji University, Seongnam, Republic of Korea.
  • Chung KW; Department of Biological Sciences, Kongju National University, Gongju, Republic of Korea.
  • Choi BO; Department of Neurology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
  • Suk K; Department of Pharmacology, Brain Science and Engineering Institute, BK21 Plus KNU Biomedical Convergence Program, School of Medicine, Kyungpook National University, Daegu, Republic of Korea.
Glia ; 68(9): 1794-1809, 2020 09.
Article en En | MEDLINE | ID: mdl-32077526

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Charcot-Marie-Tooth Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Glia Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Charcot-Marie-Tooth Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Glia Asunto de la revista: NEUROLOGIA Año: 2020 Tipo del documento: Article Pais de publicación: Estados Unidos