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Cardiac troponin T Arg92Trp mutation and progression from hypertrophic to dilated cardiomyopathy
Background: Mutations in the cardiac troponin T gene causing familial hypertrophic cardiomyopathy (HCM) are associated with a very poor prognosis but only mild hypertrophy. To date, the serial morphologic changes in patients with HCM linked to cardiac troponin T gene mutations have not been reported...
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| Publicado no: | Clin Cardiol |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Periodicals, Inc.
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6654954/ https://ncbi.nlm.nih.gov/pubmed/11346248 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.4960240510 |
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