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Complete Loss of Myelin protein zero (MPZ) in a patient with a late onset Charcot-Marie-Tooth (CMT).
Gharesouran, Jalal; Hosseinzadeh, Hassan; Naghiloo, Ali; Ghafouri-Fard, Soudeh; Hussen, Bashdar Mahmud; Taheri, Mohammad; Rezazadeh, Maryam; Samadian, Mohammad.
Afiliação
  • Gharesouran J; Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Hosseinzadeh H; Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Naghiloo A; Department of Orthopedic Surgery, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Ghafouri-Fard S; Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Hussen BM; Department of Pharmacognosy, College of Pharmacy, Hawler Medical University, Erbil, Iraq.
  • Taheri M; Urology and Nephrology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. mohammad.taheri@uni-jena.de.
  • Rezazadeh M; Institute of Human Genetics, Jena University Hospital, Jena, Germany. mohammad.taheri@uni-jena.de.
  • Samadian M; Department of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran. Rezazadehm@tbzmed.ac.ir.
Metab Brain Dis ; 38(6): 1963-1970, 2023 08.
Article em En | MEDLINE | ID: mdl-36952089
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Proteína P0 da Mielina Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Charcot-Marie-Tooth / Proteína P0 da Mielina Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article