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Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 12/2015, Volume 56, Issue 1, pp. 339 - 345
PURPOSE. To evaluate variants in the LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 genes in 298 unrelated patients with early-onset high myopia (eoHM).... 
LRPAP1 | SLC39A5 | High myopia | ZNF644 | SCO2 | REFRACTIVE ERROR | high myopia | CHINESE FAMILY | GENETIC PREDISPOSITION | RECESSIVE HIGH MYOPIA | CYTOCHROME-C-OXIDASE | DOMINANT HIGH MYOPIA | OPHTHALMOLOGY | SUSCEPTIBILITY LOCUS | HIGH-GRADE MYOPIA | HAN CHINESE | GENOME-WIDE ASSOCIATION
Journal Article
Journal Article
Molecular Vision, ISSN 1090-0535, 02/2016, Volume 22, pp. 161 - 167
Journal Article
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 03/2019, Volume 40, Issue 2, pp. 170 - 176
Background: Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous disease causing progressive degeneration of retinal photoreceptor cells.... 
hereditary X-linked recessive diseases | X-linked carrier | Retinitis pigmentosa | X-linked retinal disease | RPGR
Journal Article
Molecular Vision, ISSN 1090-0535, 02/2009, Volume 15, Issue 30-32, pp. 312 - 318
Purpose: A linkage study on autosomal recessive high myopia (arHM) has not been reported, although several loci for autosomal dominant high myopia (adHM) have... 
12Q | MAPS | BIOCHEMISTRY & MOLECULAR BIOLOGY | OPHTHALMOLOGY | GENOME-WIDE SCAN | MYP1 | 18P | CANDIDATE GENE | HIGH-GRADE MYOPIA | HONG-KONG | LOCUS | PROGRESSION | Humans | Middle Aged | Male | Myopia - pathology | Genes, Recessive | Lod Score | Myopia - genetics | Pedigree | China | Adolescent | Adult | Family | Female | Chromosomes, Human, Pair 14 - genetics | Microsatellite Repeats | Genetic Linkage
Journal Article
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