Simultaneous multi‑gene mutation screening using SNPscan in patients from ethnic minorities with nonsyndromic hearing‑impairment in Northwest China.
Autor: | SHI‑HONG DUAN1, JIAN‑LI MA1, XIAO‑LONG YANG1, YU‑FEN GUO1,2 |
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Zdroj: | Molecular Medicine Reports. Nov2017, Vol. 16 Issue 5, p6722-6728. 7p. 3 Charts, 3 Graphs. |
Databáze: | Academic Search Ultimate |
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