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Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy
Hypertrophic cardiomyopathy (HCM) is a primary disease of the cardiac muscle that occurs mainly due to mutations (>1,400 variants) in genes encoding for the cardiac sarcomere. HCM, the most common familial form of cardiomyopathy, affecting one in every 500 people in the general population, is typ...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Dove Medical Press
2014
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4199654/ https://ncbi.nlm.nih.gov/pubmed/25328416 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S49126 |
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