198 related articles for article (PubMed ID: 29934635)
1. Whole-genome sequencing reveals a recurrent missense mutation in the Connexin 46 (GJA3) gene causing autosomal-dominant lamellar cataract.
Berry V; Ionides ACW; Pontikos N; Moghul I; Moore AT; Cheetham ME; Michaelides M
Eye (Lond); 2018 May; 32(10):1661-1668. PubMed ID: 29934635
[TBL] [Abstract][Full Text] [Related]
2. A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family.
Addison PK; Berry V; Holden KR; Espinal D; Rivera B; Su H; Srivastava AK; Bhattacharya SS
Mol Vis; 2006 Jul; 12():791-5. PubMed ID: 16885921
[TBL] [Abstract][Full Text] [Related]
3. Whole Exome Sequencing Reveals Novel and Recurrent Disease-Causing Variants in Lens Specific Gap Junctional Protein Encoding Genes Causing Congenital Cataract.
Berry V; Ionides A; Pontikos N; Moghul I; Moore AT; Quinlan RA; Michaelides M
Genes (Basel); 2020 May; 11(5):. PubMed ID: 32384692
[TBL] [Abstract][Full Text] [Related]
4. Further evidence for P59L mutation in GJA3 associated with autosomal dominant congenital cataract.
Wang L; Chen Y; Chen X; Sun X
Indian J Ophthalmol; 2016 Jul; 64(7):508-12. PubMed ID: 27609163
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the GJA3 (connexin46) gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family.
Yang G; Xing B; Liu G; Lu X; Jia X; Lu X; Wang X; Yu H; Fu Y; Zhao J
Mol Vis; 2011 Apr; 17():1070-3. PubMed ID: 21552498
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract.
Jiang H; Jin Y; Bu L; Zhang W; Liu J; Cui B; Kong X; Hu L
Mol Vis; 2003 Oct; 9():579-83. PubMed ID: 14627959
[TBL] [Abstract][Full Text] [Related]
7. A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
Li Y; Wang J; Dong B; Man H
Mol Vis; 2004 Sep; 10():668-71. PubMed ID: 15448617
[TBL] [Abstract][Full Text] [Related]
8. A recurrent missense mutation in GJA3 associated with autosomal dominant cataract linked to chromosome 13q.
Bennett TM; Shiels A
Mol Vis; 2011; 17():2255-62. PubMed ID: 21897748
[TBL] [Abstract][Full Text] [Related]
9. A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family.
Guleria K; Sperling K; Singh D; Varon R; Singh JR; Vanita V
Mol Vis; 2007 Sep; 13():1657-65. PubMed ID: 17893674
[TBL] [Abstract][Full Text] [Related]
10. A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
Bennett TM; Mackay DS; Knopf HL; Shiels A
Mol Vis; 2004 Jun; 10():376-82. PubMed ID: 15208569
[TBL] [Abstract][Full Text] [Related]
11. Coralliform cataract caused by a novel connexin46 (GJA3) mutation in a Chinese family.
Zhang X; Wang L; Wang J; Dong B; Li Y
Mol Vis; 2012; 18():203-10. PubMed ID: 22312188
[TBL] [Abstract][Full Text] [Related]
12. A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree.
Ding X; Wang B; Luo Y; Hu S; Zhou G; Zhou Z; Wang J; Ma X; Qi Y
Mol Vis; 2011; 17():1343-9. PubMed ID: 21647269
[TBL] [Abstract][Full Text] [Related]
13. Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population.
Devi RR; Reena C; Vijayalakshmi P
Mol Vis; 2005 Oct; 11():846-52. PubMed ID: 16254549
[TBL] [Abstract][Full Text] [Related]
14. A novel insertional mutation in the connexin 46 (gap junction alpha 3) gene associated with autosomal dominant congenital cataract in a Chinese family.
Zhou D; Ji H; Wei Z; Guo L; Li Y; Wang T; Zhu Y; Dong X; Wang Y; He L; Xing Q; Zhang L
Mol Vis; 2013; 19():789-95. PubMed ID: 23592915
[TBL] [Abstract][Full Text] [Related]
15. Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese family.
Shen C; Wang J; Wu X; Wang F; Liu Y; Guo X; Zhang L; Cao Y; Cao X; Ma H
BMC Ophthalmol; 2017 May; 17(1):73. PubMed ID: 28526010
[TBL] [Abstract][Full Text] [Related]
16. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3).
Rees MI; Watts P; Fenton I; Clarke A; Snell RG; Owen MJ; Gray J
Hum Genet; 2000 Feb; 106(2):206-9. PubMed ID: 10746562
[TBL] [Abstract][Full Text] [Related]
17. A recurrent splice-site mutation in EPHA2 causing congenital posterior nuclear cataract.
Berry V; Pontikos N; Albarca-Aguilera M; Plagnol V; Massouras A; Prescott D; Moore AT; Arno G; Cheetham ME; Michaelides M
Ophthalmic Genet; 2018 Apr; 39(2):236-241. PubMed ID: 29039721
[TBL] [Abstract][Full Text] [Related]
18. Identification of
Li H; Jiang H; Rong R; Jiang J; Ji D; Song W; Xia X
DNA Cell Biol; 2020 Oct; 39(10):1760-1766. PubMed ID: 32808810
[TBL] [Abstract][Full Text] [Related]
19. Novel and known variants in GJA3 and LIM2 in congenital cataract families from North India.
Goyal S; Singh R; Singh JR; Vanita V
BMC Genomics; 2024 Jan; 25(1):31. PubMed ID: 38178039
[TBL] [Abstract][Full Text] [Related]
20. A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene.
Guleria K; Vanita V; Singh D; Singh JR
Mol Vis; 2007 Jun; 13():797-803. PubMed ID: 17615540
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]