Search
Skip to Search Results
Filter
Author / Creator / Contributor
Departments
Subject / Keyword
Year
Collections
Languages
Item type
-
Non-Synonymous Variants in the Premelanosome Protein (PMEL) Gene are Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Cause Biochemical Defects
DownloadFall 2018
Pigmentary Glaucoma (PG) is a common glaucoma subtype that results from release of pigment from the iris (Pigment Dispersion Syndrome) and its deposition throughout the anterior chamber of the eye. Although PG has a substantial heritable component, no causative gene variants have yet been...
1 - 1 of 1