The diagnosis of hypertrophic cardiomyopathy by cardiovascular magnetic resonance

Hypertrophic cardiomyopathy (HCM) is the most common genetic disease of the heart. HCM is characterized by a wide range of clinical expression, ranging from asymptomatic mutation carriers to sudden cardiac death as the first manifestation of the disease. Over 1000 mutations have been identified, cla...

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Bibliografiska uppgifter
Huvudupphovsmän: Noureldin, Radwa A, Liu, Songtao, Nacif, Marcelo S, Judge, Daniel P, Halushka, Marc K, Abraham, Theodore P, Ho, Carolyn, Bluemke, David A
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2012
Ämnen:
Review
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3309929/
https://ncbi.nlm.nih.gov/pubmed/22348519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1532-429X-14-17
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