Serial Observations and Mutational Analysis of an Adoptee with Family History of Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is an inherited cardiac disease with an autosomal dominant mode of transmission. Comprehensive genetic screening of several genes frequently found mutated in HCM is recommended for first-degree relatives of HCM patients. Genetic testing provides the means to identif...

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Bibliographic Details
Main Authors: Harris, Bronwyn, Pfotenhauer, Jean P., Silverstein, Cheri A., Markham, Larry W., Schafer, Kim, Exil, Vernat J., Hong, Charles C.
Format: Artigo
Language:Inglês
Published: SAGE-Hindawi Access to Research 2010
Subjects:
Case Report
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2838361/
https://ncbi.nlm.nih.gov/pubmed/20309391
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4061/2010/697269
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