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Paper Details

Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.
Mol Vis
9
2016
11p15, 14q21, 15q14, 15q25, 1p36, 2q37, 6p12, 6p21, AP3B2, CRISP3, FSCB, GJD2, GJD2 and PRSS56 genes, Illumina exome array, Myopia, NAP1L4, PRSS56, PRSS56 genes, PTCHD2, TCTE1 gene region, TCTE1 gene region at, autosomal genes, blindness, candidate genes, farsightedness, hyperopia, myopia, nearsightedness, novel variants, refractive errors, rs1550094, rs2297336, rs324146, rs634990, vision loss, visual impairment
Author NameAffiliation
Priya DuggalJohns Hopkins Bloomberg School of Public Health
Ronald KleinUniversity of Wisconsin School of Medicine and Public Health
Sudha K IyengarCase Western Reserve University
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Release 1.2