Genetic mutations in patients with nonsyndromic hearing impairment of minority and Han Chinese ethnicities in Qinghai, China

OBJECTIVE: Mutations in GJB2, SLC26A4, and mitochondrial (mt)DNA 12S rRNA genes are the main cause of nonsyndromic hearing impairment. The present study analyzed these mutations in ethnic minority and Han Chinese patients with nonsyndromic hearing impairment from Qinghai, China. METHODS: The SNPscan...

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Detalles Bibliográficos
Autores principales: Duan, Shihong, Guo, Yufen, Chen, Xingjian, Li, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Case Series
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040579/
https://www.ncbi.nlm.nih.gov/pubmed/33827324
http://dx.doi.org/10.1177/03000605211000892

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8040579/
https://www.ncbi.nlm.nih.gov/pubmed/33827324
http://dx.doi.org/10.1177/03000605211000892

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