Burden of Recurrent and Ancestral Mutations in Families With Hypertrophic Cardiomyopathy.

Ross, Samantha Barratt; Bagnall, Richard D; Ingles, Jodie; Van Tintelen, J Peter; Semsarian, Christopher

Ross, Samantha Barratt; Bagnall, Richard D; Ingles, Jodie; Van Tintelen, J Peter; Semsarian, Christopher.

Afiliação

Ross SB; From the Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Newtown, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Sydney Medical School, University of Sydney, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Department of Cardiology, Royal Prince Alfred Hospital,
Bagnall RD; From the Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Newtown, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Sydney Medical School, University of Sydney, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Department of Cardiology, Royal Prince Alfred Hospital,
Ingles J; From the Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Newtown, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Sydney Medical School, University of Sydney, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Department of Cardiology, Royal Prince Alfred Hospital,
Van Tintelen JP; From the Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Newtown, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Sydney Medical School, University of Sydney, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Department of Cardiology, Royal Prince Alfred Hospital,
Semsarian C; From the Agnes Ginges Centre for Molecular Cardiology, Centenary Institute, Newtown, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Sydney Medical School, University of Sydney, New South Wales, Australia (S.B.R., R.D.B., J.I., C.S.); Department of Cardiology, Royal Prince Alfred Hospital,

Circ Cardiovasc Genet ; 10(3)2017 Jun.

Article em En | MEDLINE | ID: mdl-28615295

Assuntos

Cardiomiopatia Hipertrófica Familiar/patologia; Adulto; Miosinas Cardíacas/genética; Cardiomiopatia Hipertrófica Familiar/genética; Proteínas de Transporte/genética; Morte Súbita Cardíaca/epidemiologia; Feminino; Estudos de Associação Genética; Haplótipos; Humanos; Masculino; Pessoa de Meia-Idade; Cadeias Pesadas de Miosina/genética; Fenótipo; Polimorfismo Genético; Recidiva

Palavras-chave

cardiomyopathy, hypertrophic; genetics; haplotypes; mutation; phenotype

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cardiomiopatia Hipertrófica Familiar Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Circ Cardiovasc Genet Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article

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