Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy‐like features

Background: Hypertrophic cardiomyopathy (HCM) is caused by mutations in the genes that encode sarcomeric proteins. Although some patients with HCM have shown dilated cardiomyopathy (DCM)‐like features, the relationship between genotype and histologic findings is not well known. Hypothesis: Family me...

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Bibliographic Details
Published in:Clin Cardiol
Main Authors: Shimizu, Masami, Ino, Hidekazu, Yamaguchi, Masato, Terai, Hidenobu, Uchiyama, Katsuharu, Inoue, Masaru, Ikeda, Masatoshi, Kawashima, Atsuhiro, Mabuchi, Hiroshi
Format: Artigo
Language:Inglês
Published: Wiley Periodicals, Inc. 2006
Subjects:
Clinical Investigations
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6654022/
https://ncbi.nlm.nih.gov/pubmed/14640471
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.4960261112
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