Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

BACKGROUND: The molecular etiology of hearing impairment in Chinese has not been thoroughly investigated. Study of GJB2 gene revealed that 30.4% of the patients with hearing loss in Inner Mongolia carried GJB2 mutations. The SLC26A4 gene mutations and relevant phenotype are analyzed in this study. M...

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Detalles Bibliográficos
Autores principales: Dai, Pu, Yuan, Yongyi, Huang, Deliang, Zhu, Xiuhui, Yu, Fei, Kang, Dongyang, Yuan, Huijun, Wu, Bailin, Han, Dongyi, Wong, Lee-Jun C
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630943/
https://www.ncbi.nlm.nih.gov/pubmed/19040761
http://dx.doi.org/10.1186/1479-5876-6-74

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630943/
https://www.ncbi.nlm.nih.gov/pubmed/19040761
http://dx.doi.org/10.1186/1479-5876-6-74

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