Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract

Li Wang; Yuhong Chen; Xueli Chen; Xinghuai Sun

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Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract

机译：与常染色体显性先天性白内障相关的GJA3中P59L突变的进一步证据

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来源
《Indian Journal of Ophthalmology》 |2016年第7期|共5页
作者
Li Wang; Yuhong Chen; Xueli Chen; Xinghuai Sun;
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中图分类眼科学;
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1. Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families [J] . Shazia Micheal, Ilse Therésia Gabri?la Niewold, Sorath Noorani Siddiqui, Genes . 2018,第2期

机译：巴基斯坦先天性白内障家族中新型GJA3常染色体隐性突变和GJA8中常染色体显性突变的描述
2. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). [J] . Rees MI, Watts P, Fenton I, Human Genetics . 2000,第2期

机译：常染色体显性先天性小带状粉状性白内障与13q11（CZP3）和连接蛋白46（GJA3）的新突变有关。
3. Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population [J] . Ramachandran Ramya DeviChandrashekar ReenaPerumalsamy Vijayalakshmi Molecular vision . 2005,第2005期

机译：GJA3的新型突变与常染色体显性先天性白内障相关的印度人口
4. Detection and Segmentation of Kidneys from Magnetic Resonance Images in Patients with Autosomal Dominant Polycystic Kidney Disease [C] . Antonio Brunetti, Giacomo Donato Cascarano, Irio De Feudis, International conference on intelligent computing . 2019

机译：常染色体显性多囊性肾脏病患者的磁共振图像肾脏检测与分割
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. Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families [O] . Shazia Micheal, Ilse Therésia Gabriëla Niewold, Sorath Noorani Siddiqui, 2018

机译：巴基斯坦先天性白内障家族中新型GJA3常染色体隐性突变和GJA8中常染色体显性突变的描述
7. Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract [O] . Li Wang, Yuhong Chen, Xueli Chen, 2016

机译：与常染色体显性先天性白内障相关的GJa3中p59L突变的进一步证据

Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract

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