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ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import.
Lin, Brian C; Phung, Trong H; Higgins, Nicole R; Greenslade, Jessie E; Prado, Miguel A; Finley, Daniel; Karbowski, Mariusz; Polster, Brian M; Monteiro, Mervyn J.
Afiliação
  • Lin BC; Program in Neuroscience, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Phung TH; Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Higgins NR; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Greenslade JE; Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Prado MA; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Finley D; Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Karbowski M; Department of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Polster BM; Program in Molecular Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
  • Monteiro MJ; Center for Biomedical Engineering and Technology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Hum Mol Genet ; 30(13): 1230-1246, 2021 06 17.
Article em En | MEDLINE | ID: mdl-33891006

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Mitocondriais / Proteínas Adaptadoras de Transdução de Sinal / Demência Frontotemporal / Proteínas Relacionadas à Autofagia / Esclerose Lateral Amiotrófica / Mitocôndrias / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Mitocondriais / Proteínas Adaptadoras de Transdução de Sinal / Demência Frontotemporal / Proteínas Relacionadas à Autofagia / Esclerose Lateral Amiotrófica / Mitocôndrias / Mutação Idioma: En Ano de publicação: 2021 Tipo de documento: Article