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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...

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Bibliografski detalji
Glavni autori: McLeod, Christopher J., Bos, J. Martijn, Theis, Jeanne L., Edwards, William D., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup: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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