Profiling of<i>WDR36</i>Missense Variants in German Patients with Glaucoma

Abstract

The occurrence of several rare putative disease-causing variants in patients with glaucoma suggests that WDR36 may be a minor disease-causing gene in glaucoma, at least in the German population. The large variability in WDR36, though, requires functional validation of these variants, once its function is characterized.