Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.

Abstract

The present study aimed to investigate the molecular etiology of nonsyndromic hearing impairment (HI) in hearing impaired populations of Hui, Tibetan, and Tu ethnicities in northwest China. A total of 283 unrelated subjects with HI who attended special education schools in northwest China were enrolled in the present study. Single-nucleotide polymorphisms… (More)
DOI: 10.3892/mmr.2017.7431

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@article{Duan2017SimultaneousMM, title={Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.}, author={Shi-Hong Duan and Jian-li Ma and Xiao-long Yang and Yu-fen Guo}, journal={Molecular medicine reports}, year={2017}, volume={16 5}, pages={6722-6728} }