Specific Changes in OCT Imaging Associated with a Novel Mutation of the RS1 Gene in X-Linked Retinoschisis.
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DOI: 10.1055/a-1901-1011
Abstract: X-linked retinoschisis (XLRS) is a rare vitreoretinal dystrophy caused by molecular genetic changes in the RS1 gene. It usually manifests itself at a young age with symmetrical splitting within different layers of the retina and… read more here.
Keywords: mutation; changes oct; rs1 gene; retinoschisis ... See more keywords