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Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is a disease of mutant sarcomeric proteins (except for phenocopy). Cardiac hypertrophy is the clinical diagnostic hallmark of HCM and a major determinant of morbidity and mortality in various cardiovascular diseases. However, there is remarkable variability in expre...

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Detalhes bibliográficos
Main Authors: Daw, E. Warwick, Chen, Suet Nee, Czernuszewicz, Grazyna, Lombardi, Raffaella, Lu, Yue, Ma, Jianzhong, Roberts, Robert, Shete, Sanjay, Marian, Ali J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2772866/
https://ncbi.nlm.nih.gov/pubmed/17652099
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddm202
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