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Cardiomyopathy, Hypertrophic, Familial

"Cardiomyopathy, Hypertrophic, Familial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.


This graph shows the total number of publications written about "Cardiomyopathy, Hypertrophic, Familial" by people in Harvard Catalyst Profiles by year, and whether "Cardiomyopathy, Hypertrophic, Familial" was a major or minor topic of these publication.
Bar chart showing 39 publications over 18 distinct years, with a maximum of 6 publications in 2002
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.