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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...
Autores principales: | Duan, Shihong, Guo, Yufen, Chen, Xingjian, Li, Yong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
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 |
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