Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: CRYBA1[original query] |
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Clinical and genetic characteristics of Chinese patients with familial or sporadic pediatric cataract. Orphanet journal of rare diseases 2018 6 13 (1): 94. Li Jingyan, Leng Yunji, Han Shirui, Yan Lulu, Lu Chaoxia, Luo Yang, Zhang Xue, Cao Lih |
Mutation screening of crystallin genes in Chinese families with congenital cataracts. Molecular vision 2019 9 25 427-437. Zhuang Jianfu, Cao Zongfu, Zhu Yihua, Liu Lijuan, Tong Yi, Chen Xiaole, Wang Yaduan, Lu Cailing, Ma Xu, Yang Juh |
A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes. Gene 2019 Jan 692 113-118. Si Nuo, Song Zixun, Meng Xiaolu, Li Xinru, Xiao Wei, Zhang X |
[Gender differences of genetic etiology in the incidence of major depressive disorder among Han freshmen]. Zhonghua yi xue za zhi 2022 5 102 (19): 1437-1444. Gao C, Luo L L, Yue S, Wang F T, Duan X M, Qian Y D, Dong Y J, Li H Y, Yue J, Xu R X, Liu Y, Gong Y |
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- Page last updated:Apr 22, 2024
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