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

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

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...

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Bibliographic Details
Main Authors: Olgu Hallioglu Kilinc, Dilek Giray, Atil Bisgin, Sevcan Tug Bozdogan, Derya Karpuz
Format: Article
Language:English
Published: KARE Publishing 2017-07-01
Series:Türk Kardiyoloji Derneği Arşivi
Subjects:
echocardiography
hypertrophic cardiomyopathy
molecular genetics
mybpc.
Online Access:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-56267

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https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tkd&un=TKDA-56267

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