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Genetic mutations in nonsyndromic deafness patients of Chinese minority and han ethnicities in Yunnan, China
BACKGROUND: Each year in China, 30,000 babies are born with congenital hearing impairment. However, the molecular etiology of hearing impairment in the Yunnan Province population where more than 52 minorities live has not been thoroughly investigated. To provide appropriate genetic testing and couns...
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| Main Authors: | , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2013
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3878508/ https://ncbi.nlm.nih.gov/pubmed/24341454 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-11-312 |
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