Cargando...
Identification of a novel mutation in CRYM in a Chinese family with hearing loss using whole-exome sequencing
Previous studies have identified ~50 genes that contribute to non-syndromic autosomal dominant sensorineural deafness (DFNA). However, in numerous families with hearing loss, the specific gene mutation remains to be identified. In the present study, the clinical characteristics and gene mutations we...
Gardado en:
| Publicado en: | Exp Ther Med |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
D.A. Spandidos
2020
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7388290/ https://ncbi.nlm.nih.gov/pubmed/32742378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2020.8890 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|