Xukun Yan

A novel mutation in the MITF may be digenic with GJB2 mutations in a large Chinese family of Waardenburg syndrome type II.

Hongyan Wang, Duan Ma, Huawei Li, 2011, Journal of genetics and genomics = Yi chuan xue bao.

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome

Weiwei Guo, Ping Chen, Hui Jiang, 2014, Cell Research.

Early cretaceous bimodal volcanic rocks in Wuga Co area, central tibet: The first identification of direct products derived from slab sinking in the Bangong-Nujiang suture zone

Ming Zheng, Yi‐Ling Hu, Zhi‐Bo Liu, 2023, Frontiers in Earth Science.

Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene

Shan Sun, Yingzi He, Huawei Li, 2011, Journal of Medical Genetics.

Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11)

Huan Wang, Duan Ma, Huawei Li, 2013, PloS one.

A novel mutation in the MITF may be digenic with GJB2 mutations in a large Chinese family of Waardenburg syndrome type II.

Hongyan Wang, Duan Ma, Huawei Li, 2011, Journal of genetics and genomics = Yi chuan xue bao.

Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene

Shan Sun, Yingzi He, Huawei Li, 2011, Journal of Medical Genetics.