Compound Heterozygous Variants of the CPAMD8 Gene Co-Segregating in Two Chinese Pedigrees With Pigment Dispersion Syndrome/Pigmentary Glaucoma
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DOI: 10.3389/fgene.2022.845081
Abstract: The molecular mechanisms underlying the pathogenesis of pigment dispersion syndrome and pigmentary glaucoma remain unclear. In pedigree-based studies, familial aggregation and recurrences in relatives suggest a strong genetic basis for pigmentary glaucoma. In this study,… read more here.
Keywords: glaucoma; dispersion syndrome; pigmentary glaucoma; pigment dispersion ... See more keywords