A carregar...
Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss
Variants of KCNQ4 are one of the most common causes of dominantly inherited nonsyndromic hearing loss. We investigated a consanguineous family in which two individuals had prelignual hearing loss, apparently inherited in a recessive mode. Whole-exome sequencing analyses demonstrated genetic heteroge...
Na minha lista:
| Publicado no: | Gene |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7709079/ https://ncbi.nlm.nih.gov/pubmed/31028865 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gene.2019.04.064 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|