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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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Main Authors: | , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2007
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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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