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A Novel Homozygous Intronic Variant in TNNT2 Associates With Feline Cardiomyopathy
BackgroundHypertrophic 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 how...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Frontiers Media S.A.
2020-11-01
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| Serie: | Frontiers in Physiology |
| Soggetti: | |
| Accesso online: | https://www.frontiersin.org/articles/10.3389/fphys.2020.608473/full |
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