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TBX20 loss-of-function variants in families with left ventricular non-compaction cardiomyopathy.
Chang, Yuchen; Wacker, Julie; Ingles, Jodie; Macciocca, Ivan; King, Ingrid; Semsarian, Christopher; McGaughran, Julie; Weintraub, Robert G; Bagnall, Richard D.
Afiliação
  • Chang Y; Bioinformatics and Molecular Genetics at Centenary Institute, The University of Sydney, Sydney, New South Wales, Australia.
  • Wacker J; Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
  • Ingles J; Department of Cardiology, The Royal Children's Hospital Melbourne, Parkville, Victoria, Australia.
  • Macciocca I; Faculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
  • King I; Centre for Population Genomics, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.
  • Semsarian C; Department of Cardiology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.
  • McGaughran J; Clinical Sciences, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Weintraub RG; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
  • Bagnall RD; Clinical Sciences, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
J Med Genet ; 61(2): 171-175, 2024 Jan 19.
Article em En | MEDLINE | ID: mdl-37657916
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiopatias Congênitas / Insuficiência Cardíaca / Cardiomiopatias Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cardiopatias Congênitas / Insuficiência Cardíaca / Cardiomiopatias Idioma: En Ano de publicação: 2024 Tipo de documento: Article