Association of FOXE3-p.Ala170Ala and PITX3-p.Ile95Ile Polymorphisms with Congenital Cataract and Microphthalmia

机译：FOXE3-p.Ala170Ala和PITX3-p.Ile95Ile多态性与先天性白内障和小眼症的关联

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摘要

Purpose:To investigate the association of FOXE3-p.Ala170Ala (rs34082359) and PITX3-p.Ile95Ile (rs2281983) polymorphisms with congenital cataract and microphthalmia in a western Indian population.

机译：目的：研究印度西部人群FOXE3-p.Ala170Ala（rs34082359）和PITX3-p.Ile95Ile（rs2281983）多态性与先天性白内障和小眼症的关系。

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期刊名称 Journal of Ophthalmic Vision Research
作者
Nair Gopinathan Vidya; Darshini Ganatra; Abhay R. Vasavada; Sankaranarayanan Rajkumar;
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作者单位

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年(卷),期 2018(13),4
年度 2018
页码 397–402
总页数 6
原文格式 PDF
正文语种
中图分类眼科学;
关键词
Congenital Cataract Forkhead Box E3 Microphthalmia Paired-like Domain Transcription Factor 3;

机译：先天性白内障;额头盒E3;小眼症;配对样域转录因子3;

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专利

1. Association of FOXE3-p.Ala170Ala and PITX3-p.Ile95Ile polymorphisms with congenital cataract and microphthalmia [J] . Nair Gopinathan Vidya, Darshini Ganatra, Abhay R Vasavada, Journal of Ophthalmic and Vision Research . 2018,第4期

机译：FOXE3-p.Ala170Ala和PITX3-p.Ile95Ile多态性与先天性白内障和小眼症的关联
2. Evaluating the association of bone morphogenetic protein 4-V152A and SIX homeobox 6-H141N polymorphisms with congenital cataract and microphthalmia in Western Indian population [J] . Vidya N. G., Vasavada A. R., Rajkumar S. Journal of postgraduate medicine . 2018,第2期

机译：评估骨形态发生蛋白4-V152a和六种Homeobox 6-H141n多态性与西部印度人群中的先天性白内障和微蛋白的关联
3. Evaluating the association of bone morphogenetic protein 4-V152A and SIX homeobox 6-H141N polymorphisms with congenital cataract and microphthalmia in Western Indian population [J] . NG Vidya, AR Vasavada, S Rajkumar Journal of postgraduate medicine. . 2018,第2期

机译：在印度西部人群中评估骨形态发生蛋白4-V152A和SIX同源盒6-H141N多态性与先天性白内障和小眼症的关联
4. Low Vision Assessment and Management of a Congenital Aniridia and Associated Cataract [C] . Mariah Joan F. Chiong, Emmanuel T. Gasolasco Bakti Tunas Husada-Health Science International Conference . 2020

机译：低视力评估和对先天性Aniridia和相关性白内障的管理
5. Genomic study and mutation functional analysis of autosomal dominant congenital cataract. [D] . Zhang, Liyun. 2007

机译：常染色体显性先天性白内障的基因组研究和突变功能分析。
6. Unique presentation of congenital cataract concurrent with microcornea microphthalmia plus posterior capsule defect in monozygotic twins caused by a novel GJA8 mutation [O] . Hongfang Zhang, Zhenji Chen, Kaiwen He, 2019

机译：由新的GJA8突变引起的单卵双胞胎先天性白内障并发微角膜小眼症和后囊缺损的独特表现
7. Association of FOXE3-p.Ala170Ala and PITX3-p.Ile95Ile polymorphisms with congenital cataract and microphthalmia [O] . Sankaranarayanan Rajkumar, NairGopinathan Vidya, Darshini Ganatra, 2018

机译：Foxe3-P.Ala170Ala和PitX3-P.ILE95与先天性白内障和微蛋白的关联

Association of FOXE3-p.Ala170Ala and PITX3-p.Ile95Ile Polymorphisms with Congenital Cataract and Microphthalmia

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