GWAS identifies two common loci associated with pigment dispersion syndrome/pigmentary glaucoma and implicate myopia in its development.
Simcoe MJ, Shah A, Fan B et al.
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Abstract
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Purpose: To identify genetic variants associated with pigment dispersion syndrome (PDS) and pigmentary glaucoma (PG) in unrelated patients and to further understand the genetic and potentially causal relationships between PDS and associated risk factors.
179 Pigment dispersion syndrome European ancestry cases, 395 pigmentary glaucoma European ancestry cases, 52,627 European ancestry controls
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