Načítá se...
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...
Uloženo v:
| Hlavní autoři: | , , , |
|---|---|
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2020-11-01
|
| Edice: | Frontiers in Physiology |
| Témata: | |
| On-line přístup: | https://www.frontiersin.org/articles/10.3389/fphys.2020.608473/full |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|