Novel dilated cardiomyopathy associated to Calreticulin and Myo7A gene mutation in Usher syndrome
Abstract We report a novel cardiomyopathy associated to Usher syndrome and related to combined mutation of MYO7A and Calreticulin genes. A 37‐year‐old man with deafness and vision impairment because of retinitis pigmentosa since childhood and a MYO7A gene mutation suggesting Usher syndrome, develope...
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| Principais autores: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2021-06-01
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| coleção: | ESC Heart Failure |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1002/ehf2.13260 |
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