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A Novel Homozygous Intronic Variant in TNNT2 Associates With Feline Cardiomyopathy
BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a genetic disease of the heart and the most common cause of sudden cardiac death in the young. HCM is considered a disease of the sarcomere owing to the large number of mutations in genes encoding sarcomeric proteins. The riddle lies in discovering ho...
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| Publicado no: | Front Physiol |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7701303/ https://ncbi.nlm.nih.gov/pubmed/33304277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2020.608473 |
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