All individuals with variants in gene CPAMD8

2 entries on 1 page. Showing entries 1 - 2.
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00331853 15DG0621 PubMed: Alsaif 2019 sporadic - - Saudi Arabia - - - - - retinal disease primary congenital glaucoma, lens subluxation 1 1 LOVD
00392258 3 PubMed: Bell 2021 - F yes (United Kingdom (Great Britain)) - - - - - retinal disease Posterior subcapsular cataract, anterior segment dysgenesis, pupillary abnormalities including ectopic pupils, ectropion nuvae and irodensis, nystagmus, dysplastic optic discs, large corneal diameters 1 1 LOVD
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