The Genetic Mutation of <i>ANO5</i> in Rabbits Recapitulates Human Cardiomyopathy
The limb girdle muscular dystrophy type 2L (LGMD2L) is caused by mutations of the <i>ANO5</i> gene in humans which encodes a 913 amino-acid integral membrane protein. Although cardiomyopathy has been reported in patients with an <i>ANO5</i> mutation, the <i>ANO5</i&g...
| Główni autorzy: | , , , , , |
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| Format: | Artykuł |
| Język: | English |
| Wydane: |
MDPI AG
2020-07-01
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| Seria: | Applied Sciences |
| Hasła przedmiotowe: | |
| Dostęp online: | https://www.mdpi.com/2076-3417/10/14/4976 |