Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia.

van der Zwaag, P A; Cox, M G P J; van der Werf, C; Wiesfeld, A C P; Jongbloed, J D H; Dooijes, D; Bikker, H; Jongbloed, R; Suurmeijer, A J H; van den Berg, M P; Hofstra, R M W; Hauer, R N W; Wilde, A A M; van Tintelen, J P

van der Zwaag, P A; Cox, M G P J; van der Werf, C; Wiesfeld, A C P; Jongbloed, J D H; Dooijes, D; Bikker, H; Jongbloed, R; Suurmeijer, A J H; van den Berg, M P; Hofstra, R M W; Hauer, R N W; Wilde, A A M; van Tintelen, J P.

Afiliação

van der Zwaag PA; Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Neth Heart J ; 18(12): 583-91, 2010 Dec.

Article em En | MEDLINE | ID: mdl-21301620

Palavras-chave

ARVC/D; Cardiomyopathy; Founder Mutation; Genetics; PKP2

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Problema de saúde: 6_cardiovascular_diseases / 6_other_circulatory_diseases Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Neth Heart J Ano de publicação: 2010 Tipo de documento: Article País de afiliação: Holanda

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