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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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Detaylı Bibliyografya
Asıl Yazarlar: McLeod, Christopher J., Bos, J. Martijn, Theis, Jeanne L., Edwards, William D., Gersh, Bernard J., Ommen, Steve R., Ackerman, Michael J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2009
Konular:
Online Erişim: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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