Common Molecular Etiologies Are Rare in Nonsyndromic Tibetan Chinese Patients with Hearing Impairment

BACKGROUND: Thirty thousand infants are born every year with congenital hearing impairment in mainland China. Racial and regional factors are important in clinical diagnosis of genetic deafness. However, molecular etiology of hearing impairment in the Tibetan Chinese population living in the Tibetan...

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Detalles Bibliográficos
Autores principales: Yuan, Yongyi, Zhang, Xun, Huang, Shasha, Zuo, Lujie, Zhang, Guozheng, Song, Yueshuai, Wang, Guojian, Wang, Hongtian, Huang, Deliang, Han, Dongyi, Dai, Pu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289614/
https://www.ncbi.nlm.nih.gov/pubmed/22389666
http://dx.doi.org/10.1371/journal.pone.0030720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289614/
https://www.ncbi.nlm.nih.gov/pubmed/22389666
http://dx.doi.org/10.1371/journal.pone.0030720

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