Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Keratoconus and DOCK9[original query] |
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Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus. European journal of human genetics : EJHG 2012 Apr 20 (4): 389-97. Czugala Marta, Karolak Justyna A, Nowak Dorota M, Polakowski Piotr, Pitarque Jose, Molinari Andrea, Rydzanicz Malgorzata, Bejjani Bassem A, Yue Beatrice Y J T, Szaflik Jacek P, Gajecka Marze |
Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification. Ophthalmic genetics 2015 Aug 1-7. Karolak Justyna A, Polakowski Piotr, Szaflik Jerzy, Szaflik Jacek P, Gajecka Marze |
Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population. Molecular vision 2017 23 296-305. Yu Xiaoning, Chen Binbin, Zhang Xin, Shentu Xingch |
Novel Mutations Identified in the Chinese Han Population with Keratoconus by Next-Generation Sequencing. Journal of ophthalmology 2022 2 2022 9991910. Chen Binbin, Yu Xiaoning, Zhang Xin, Yang Hao, Cui Yilei, Shentu Xingch |
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- Page last updated:Apr 22, 2024
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