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Mutation analysis of SOD1, C9orf72, TARDBP and FUS genes in ethnically-diverse Malaysian patients with amyotrophic lateral sclerosis (ALS).
Edgar, Suzanna; Ellis, Melina; Abdul-Aziz, Nur Adilah; Goh, Khean-Jin; Shahrizaila, Nortina; Kennerson, Marina L; Ahmad-Annuar, Azlina.
Afiliação
  • Edgar S; Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Ellis M; Northcott Neuroscience Laboratory, ANZAC Research Institute, University of Sydney, Concord, New South Wales, Australia.
  • Abdul-Aziz NA; Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Goh KJ; Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Shahrizaila N; Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
  • Kennerson ML; Northcott Neuroscience Laboratory, ANZAC Research Institute, University of Sydney, Concord, New South Wales, Australia; Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia; Molecular Medicine Laboratory, Concord Hospital, Concord, New South Wales, Australia. Electronic ad
  • Ahmad-Annuar A; Department of Biomedical Science, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: azlina_aa@um.edu.my.
Neurobiol Aging ; 108: 200-206, 2021 12.
Article em En | MEDLINE | ID: mdl-34404558
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína FUS de Ligação a RNA / Proteínas de Ligação a DNA / Estudos de Associação Genética / Superóxido Dismutase-1 / Proteína C9orf72 / Esclerose Lateral Amiotrófica / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteína FUS de Ligação a RNA / Proteínas de Ligação a DNA / Estudos de Associação Genética / Superóxido Dismutase-1 / Proteína C9orf72 / Esclerose Lateral Amiotrófica / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article