Sign Up to like & get
recommendations!
0
Published in 2017 at "Journal of Cellular and Molecular Medicine"
DOI: 10.1111/jcmm.13019
Abstract: X‐linked juvenile retinoschisis (XLRS) is a hereditary retinal dystrophy in young males, caused by mutations in the RS1 gene. The function of the encoded protein, termed retinoschisin, and the molecular mechanisms underlying XLRS pathogenesis are…
read more here.
Keywords:
apoptosis;
kinase;
kinase signalling;
linked juvenile ... See more keywords