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Mutation analysis of common deafness genes among 1,201 patients with non‐syndromic hearing loss in Shanxi Province
BACKGROUND: Hearing impairment is one of most frequent birth defects, which affects nearly 1 in every 1,000 live births. However, the molecular etiology of non‐syndromic deafness in China is not well studied. Here, we have investigated the presence of mutations in three genes commonly mutated in non...
| Autores principales: | , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418354/ https://www.ncbi.nlm.nih.gov/pubmed/30693673 http://dx.doi.org/10.1002/mgg3.537 |