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Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families.
Kediha, M I; Tazir, M; Magnouche, C; Sternberg, D; Belarbi, S; Eymard, B; Ali Pacha, L.
Afiliação
  • Kediha MI; Neurology department, Mustapha Bacha university Hospital, Algiers, Algeria. Electronic address: kediha.islam@gmail.com.
  • Tazir M; Neurology department, Mustapha Bacha university Hospital, Algiers, Algeria.
  • Magnouche C; Neurology department, Ali Ait Idir university Hospital, Algiers, Algeria.
  • Sternberg D; Myogenetics laboratory, Pitié Salpetriere university hospital, Paris, France.
  • Belarbi S; Neurology department, Ali Ait Idir university Hospital, Algiers, Algeria.
  • Eymard B; Neurology department, Pitié Saleptriere university hospital, Paris, France.
  • Ali Pacha L; Neurology department, Mustapha Bacha university Hospital, Algiers, Algeria.
Rev Neurol (Paris) ; 179(6): 570-575, 2023 Jun.
Article em En | MEDLINE | ID: mdl-36764859
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Miastênicas Congênitas 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: Síndromes Miastênicas Congênitas Idioma: En Ano de publicação: 2023 Tipo de documento: Article