Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: CRYBA4[original query] |
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Mutational screening of 10 genes in Chinese patients with microphthalmia and/or coloboma. Molecular vision 2009 15 . Zhang Xiaohui, Li Shiqiang, Xiao Xueshan, Jia Xiaoyun, Wang Panfeng, Shen Huangxuan, Guo Xiangming, Zhang Qingjio |
Association of high myopia with crystallin beta A4 (CRYBA4) gene polymorphisms in the linkage-identified MYP6 locus. PloS one 2012 7 (6): 6. Ho DW, Yap MK, Ng PW, Fung WY, Yip SP |
Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma. International journal of molecular medicine 2015 Oct 36 (4): 1111-7. Huang Xiaobo, Xiao Xueshan, Jia Xiaoyun, Li Shiqiang, Li Miaoling, Guo Xiangming, Liu Xing, Zhang Qingjio |
A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts. PloS one 2016 11 (6): e0157005. Jiao Xiaodong, Kabir Firoz, Irum Bushra, Khan Arif O, Wang Qiwei, Li David, Khan Asma A, Husnain Tayyab, Akram Javed, Riazuddin Sheikh, Hejtmancik J Fielding, Riazuddin S Am |
Associations between CRYBA4 gene variants and high myopia in a Japanese population. Clinical ophthalmology (Auckland, N.Z.) 2017 11 2151-2156. Kawagoe Tatsukata, Ota Masao, Meguro Akira, Takeuchi Masaki, Yamane Takahiro, Shimazaki Haruna, Takeuchi Masaru, Okada Eiichi, Teshigawara Takeshi, Mizuki Nobuhi |
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 |
Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia. Ophthalmic genetics 2018 Feb 1-9. Vidya Nair Gopinathan, Rajkumar Sankaranarayanan, Vasavada Abhay |
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 |
Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian journal of ophthalmology 2021 Aug 69 (8): 2064-2070. Nair Vidya, Sankaranarayanan Rajkumar, Vasavada Abhay Raghuka |
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- Page last updated:Apr 22, 2024
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