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Clinical and functional characterization of TNNT2 mutations identified in patients with dilated cardiomyopathy
BACKGROUND: A key issue for cardiovascular genetic medicine is ascertaining if a putative mutation indeed causes dilated cardiomyopathy (DCM). This is critically important as genetic DCM, usually presenting with advanced, life-threatening disease, may be preventable with early intervention in relati...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2900844/ https://ncbi.nlm.nih.gov/pubmed/20031601 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.108.846733 |
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