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Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy.
Smith, Sarah J; Fabian, Lacramioara; Sheikh, Adeel; Noche, Ramil; Cui, Xiucheng; Moore, Steven A; Dowling, James J.
Affiliation
  • Smith SJ; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada.
  • Fabian L; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Sheikh A; Department of Family Medicine, University of Calgary, Calgary T2R 0X7, Alberta.
  • Noche R; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Cui X; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
  • Moore SA; Schulich School of Medicine and Dentistry, Western University, London, ON N6A 5C1, Canada.
  • Dowling JJ; Program for Genetics & Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Hum Mol Genet ; 31(5): 733-747, 2022 03 03.
Article in En | MEDLINE | ID: mdl-34568901
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Zebrafish / Muscular Dystrophies Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: Canada Country of publication: United kingdom
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Zebrafish / Muscular Dystrophies Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2022 Document type: Article Affiliation country: Canada Country of publication: United kingdom