» Articles » PMID: 28085539

Mutations in DZIP1 and XYLT1 Are Associated with Nonsyndromic Early Onset High Myopia in the Korean Population

Overview
Publisher Informa Healthcare
Specialties Genetics
Ophthalmology
Date 2017 Jan 14
PMID 28085539
Citations 7
Authors
Affiliations
Soon will be listed here.
Citing Articles

De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia.

Huang X, Li H, Yang S, Ma M, Lian Y, Wu X BMC Med Genomics. 2024; 17(1):142.

PMID: 38790056 PMC: 11127418. DOI: 10.1186/s12920-024-01904-9.


Whole-Exome Sequencing Among School-Aged Children With High Myopia.

Yu X, Yuan J, Chen Z, Li K, Yao Y, Xing S JAMA Netw Open. 2023; 6(12):e2345821.

PMID: 38039006 PMC: 10692858. DOI: 10.1001/jamanetworkopen.2023.45821.


Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families.

Zi F, Li Z, Cheng W, Huang X, Sheng X, Rong W BMC Med Genomics. 2023; 16(1):223.

PMID: 37749571 PMC: 10521526. DOI: 10.1186/s12920-023-01665-x.


Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia.

Yang E, Yu J, Liu X, Chu H, Li L Invest Ophthalmol Vis Sci. 2023; 64(5):10.

PMID: 37191617 PMC: 10198284. DOI: 10.1167/iovs.64.5.10.


Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China.

Ye M, Ma Y, Qin Y, Cai B, Ma L, Ma Z Mol Genet Genomics. 2023; 298(3):669-682.

PMID: 36964802 DOI: 10.1007/s00438-023-02003-7.