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Targeted next generation sequencing identified novel mutations in RPGRIP1 associated with both retinitis pigmentosa and Leber's congenital amaurosis in unrelated Chinese patients 期刊论文
2017, 卷号: 8, 期号: 21, 页码: 35176
作者:  Huang, Hui[1];  Wang, Ying[2,3];  Chen, Huishuang[1];  Chen, Yanhua[1,4];  Wu, Jing[1]
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