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Autopsy findings in siblings with hypertrophic cardiomyopathy caused by Arg92Trp mutation in the cardiac troponin T gene showing dilated cardiomyopathy‐like features
Background: Hypertrophic cardiomyopathy (HCM) is caused by mutations in the genes that encode sarcomeric proteins. Although some patients with HCM have shown dilated cardiomyopathy (DCM)‐like features, the relationship between genotype and histologic findings is not well known. Hypothesis: Family me...
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| Publicado no: | Clin Cardiol |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Periodicals, Inc.
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6654022/ https://ncbi.nlm.nih.gov/pubmed/14640471 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.4960261112 |
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