top of page
Search
A Novel ARL3 Gene Mutation Associated With Autosomal Dominant Retinal Degeneration
Our results . . . augment the evidence that the ARL3 gene is another cause of non-syndromic retinal degeneration.
Dec 31, 2021
Dominant ARL3-related retinitis pigmentosa
Study confirms that the ARL3 missense variant p.(Tyr90Cys) causes retinitis pigmentosa.
Apr 1, 2019
ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting
In this study, we sought to determine the functional network of INPP5E and the mechanisms by which INPP5E is targeted to primary cilia.
Nov 27, 2012
All Posts
bottom of page