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HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy.
Clin Chem Lab Med ; 54(7): 1161-7, 2016 Jul 01.
Article in En | MEDLINE | ID: mdl-26581070

Full text: 1 Database: MEDLINE Main subject: Cardiomyopathy, Dilated / Genetic Predisposition to Disease / Basic Helix-Loop-Helix Transcription Factors / Mutation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Female / Humans / Male / Middle aged Language: En Journal: Clin Chem Lab Med Journal subject: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2016 Type: Article

Full text: 1 Database: MEDLINE Main subject: Cardiomyopathy, Dilated / Genetic Predisposition to Disease / Basic Helix-Loop-Helix Transcription Factors / Mutation Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Animals / Female / Humans / Male / Middle aged Language: En Journal: Clin Chem Lab Med Journal subject: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2016 Type: Article