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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...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2020
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| Assuntos: | |
| Acesso em linha: | 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 |
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