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42. Novel compound heterozygous mutations in MYO7A Associated with Usher syndrome 1 in a Chinese family. Gao X; Wang GJ; Yuan YY; Xin F; Han MY; Lu JQ; Zhao H; Yu F; Xu JC; Zhang MG; Dong J; Lin X; Dai P PLoS One; 2014; 9(7):e103415. PubMed ID: 25080338 [TBL] [Abstract][Full Text] [Related]
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