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Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic kadazandusun family.
Tan, Joo-San; Ambang, Tomica; Ahmad-Annuar, Azlina; Rajahram, Giri Shan; Wong, Kum Thong; Goh, Khean Jin.
Afiliação
  • Tan JS; Division of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Ambang T; Division of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Ahmad-Annuar A; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Rajahram GS; Department of Medicine, Hospital Queen Elizabeth, Kota Kinabalu, Sabah, Malaysia.
  • Wong KT; Department of Pathology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Goh KJ; Division of Neurology, Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Muscle Nerve ; 53(5): 822-6, 2016 May.
Article em En | MEDLINE | ID: mdl-26789281
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Colina O-Acetiltransferase / Síndromes Miastênicas Congênitas / Heterozigoto Limite: Adult / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Muscle Nerve Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linhagem / Colina O-Acetiltransferase / Síndromes Miastênicas Congênitas / Heterozigoto Limite: Adult / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Muscle Nerve Ano de publicação: 2016 Tipo de documento: Article