Llwytho...

Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations

BACKGROUND: Between 30% and 60% of clinical cases of hypertrophic cardiomyopathy (HC) can be attributed to mutations in the genes encoding cardiac myofilament proteins. Interestingly, it appears that the likelihood of an underlying myofilament mutation can be predicted by echocardiographic assessmen...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: McLeod, Christopher J., Bos, J. Martijn, Theis, Jeanne L., Edwards, William D., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2009
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC3281581/
https://ncbi.nlm.nih.gov/pubmed/19853701
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ahj.2009.09.006
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