Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene

• Egile Nagusiak: Olgu Hallioglu Kilinc (Egilea), Dilek Giray (Egilea), Atil Bisgin (Egilea), Sevcan Tug Bozdogan (Egilea), Derya Karpuz (Egilea)
• Formatua: Liburua
• Argitaratua: KARE Publishing, 2017-07-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

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 hav...