Article
Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene.
Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir - 1 Jul 2017
Hallıoğlu Kılınç Olgu, Giray Dilek, Bişgin Atıl, Tuğ Bozdoğan Sevcan, Karpuz Derya
Abstract excerpt
Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease with variable clinical features that is inherited as autosomal dominant with variable penetrance. Recent developments in genetics of hereditary cardiomyopathy have not only enlightened many points about pathogenesis, but have also provided great benefit to diagnostic approaches of clinicians. Heterozygous mutation of c3691-3692insTTCA in...
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