211 related articles for article (PubMed ID: 21423867)
1. A novel GPR143 splicing mutation in a Chinese family with X-linked congenital nystagmus.
Hu J; Liang D; Xue J; Liu J; Wu L
Mol Vis; 2011 Mar; 17():715-22. PubMed ID: 21423867
[TBL] [Abstract][Full Text] [Related]
2. Novel GPR143 mutations and clinical characteristics in six Chinese families with X-linked ocular albinism.
Fang S; Guo X; Jia X; Xiao X; Li S; Zhang Q
Mol Vis; 2008; 14():1974-82. PubMed ID: 18978956
[TBL] [Abstract][Full Text] [Related]
3. GPR143 Gene Mutations in Five Chinese Families with X-linked Congenital Nystagmus.
Han R; Wang X; Wang D; Wang L; Yuan Z; Ying M; Li N
Sci Rep; 2015 Jul; 5():12031. PubMed ID: 26160353
[TBL] [Abstract][Full Text] [Related]
4.
Zhong J; You B; Xu K; Zhang X; Xie Y; Li Y
Ophthalmic Genet; 2021 Dec; 42(6):717-724. PubMed ID: 34346269
[TBL] [Abstract][Full Text] [Related]
5. A previously unidentified deletion in G protein-coupled receptor 143 causing X-linked congenital nystagmus in a Chinese family.
Liu J; Jia Y; Wang L; Bu J
Indian J Ophthalmol; 2016 Nov; 64(11):813-817. PubMed ID: 27958203
[TBL] [Abstract][Full Text] [Related]
6. A novel splicing site mutation of the GPR143 gene in a Chinese X-linked ocular albinism pedigree.
Cai CY; Zhu H; Shi W; Su L; Shi O; Cai CQ; Ling C; Li WD
Genet Mol Res; 2013 Nov; 12(4):5673-9. PubMed ID: 24301936
[TBL] [Abstract][Full Text] [Related]
7. Screening of TYR, OCA2, GPR143, and MC1R in patients with congenital nystagmus, macular hypoplasia, and fundus hypopigmentation indicating albinism.
Preising MN; Forster H; Gonser M; Lorenz B
Mol Vis; 2011 Apr; 17():939-48. PubMed ID: 21541274
[TBL] [Abstract][Full Text] [Related]
8. A novel GPR143 duplication mutation in a Chinese family with X-linked congenital nystagmus.
Peng Y; Meng Y; Wang Z; Qin M; Li X; Dian Y; Huang S
Mol Vis; 2009; 15():810-4. PubMed ID: 19390656
[TBL] [Abstract][Full Text] [Related]
9. A novel splicing mutation of the FRMD7 gene in a Chinese family with X-linked congenital nystagmus.
Hu Y; Shen J; Zhang S; Yang T; Huang S; Yuan H
Mol Vis; 2012; 18():87-91. PubMed ID: 22262942
[TBL] [Abstract][Full Text] [Related]
10.
Xu J; Zheng Y; Cheng L; Sun H; Yu X; Gu F; Song E
Mol Vis; 2023; 29():234-244. PubMed ID: 38222445
[TBL] [Abstract][Full Text] [Related]
11. Identification of a novel GPR143 deletion in a Chinese family with X-linked congenital nystagmus.
Zhou P; Wang Z; Zhang J; Hu L; Kong X
Mol Vis; 2008 May; 14():1015-9. PubMed ID: 18523664
[TBL] [Abstract][Full Text] [Related]
12. A novel nonsense mutation of the GPR143 gene identified in a Chinese pedigree with ocular albinism.
Yan N; Liao X; Cai SP; Lan C; Wang Y; Zhou X; Yin Y; Yu W; Liu X
PLoS One; 2012; 7(8):e43177. PubMed ID: 22916221
[TBL] [Abstract][Full Text] [Related]
13. Iris hyperpigmentation in a Chinese family with ocular albinism and the GPR143 mutation.
Xiao X; Zhang Q
Am J Med Genet A; 2009 Aug; 149A(8):1786-8. PubMed ID: 19610097
[TBL] [Abstract][Full Text] [Related]
14. Molecular genetic analysis of patients with sporadic and X-linked infantile nystagmus.
Zhao H; Huang XF; Zheng ZL; Deng WL; Lei XL; Xing DJ; Ye L; Xu SZ; Chen J; Zhang F; Yu XP; Jin ZB
BMJ Open; 2016 Apr; 6(4):e010649. PubMed ID: 27036142
[TBL] [Abstract][Full Text] [Related]
15. A novel GPR143 mutation in a Chinese family with X‑linked ocular albinism type 1.
Gao X; Liu T; Cheng X; Dai A; Liu W; Li R; Zhang M
Mol Med Rep; 2020 Jan; 21(1):240-248. PubMed ID: 31746431
[TBL] [Abstract][Full Text] [Related]
16. Identification of a novel
Jung JH; Oh EH; Shin JH; Kim HS; Choi SY; Choi KD; Lee C; Choi JH
J Genet; 2018 Dec; 97(5):1479-1484. PubMed ID: 30555098
[TBL] [Abstract][Full Text] [Related]
17. Investigation of the gene mutations in two Chinese families with X-linked infantile nystagmus.
Li N; Wang X; Wang Y; Wang L; Ying M; Han R; Liu Y; Zhao K
Mol Vis; 2011 Feb; 17():461-8. PubMed ID: 21365021
[TBL] [Abstract][Full Text] [Related]
18. A novel missense mutation in the FERM domain containing 7 (FRMD7) gene causing X-linked idiopathic congenital nystagmus in a Chinese family.
Liu Z; Mao S; Pu J; Ding Y; Zhang B; Ding M
Mol Vis; 2013; 19():1834-40. PubMed ID: 23946638
[TBL] [Abstract][Full Text] [Related]
19. Deletion in the OA1 gene in a family with congenital X linked nystagmus.
Preising M; Op de Laak JP; Lorenz B
Br J Ophthalmol; 2001 Sep; 85(9):1098-103. PubMed ID: 11520764
[TBL] [Abstract][Full Text] [Related]
20. A novel frameshift mutation in FRMD7 causes X-linked infantile nystagmus in a Chinese family.
Chen J; Wei Y; Tian L; Kang X
BMC Med Genet; 2019 Jan; 20(1):5. PubMed ID: 30616528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]