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Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy

Background: Mutations in the cardiac troponin T gene causing familial hypertrophic cardiomyopathy (HCM) are associated with a very poor prognosis but only mild hypertrophy. To date, the serial morphologic changes in patients with HCM linked to cardiac troponin T gene mutations have not been reported...

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Bibliografiske detaljer
Udgivet i:Clin Cardiol
Main Authors: Fujino, Noboru, Shimizu, Masami, Ino, Hidekazu, Okeie, Kazuyasu, Yamaguchi, Masato, Yasuda, Toshihiko, Kokado, Hiromasa, Mabuchi, Hiroshi
Format: Artigo
Sprog:Inglês
Udgivet: Wiley Periodicals, Inc. 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6654954/
https://ncbi.nlm.nih.gov/pubmed/11346248
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.4960240510
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