Author:
Sundaresan Periasamy,Mishra Chitaranjan,Duvesh Roopam,Chowdhury Susmita,Anjanamurthy Rupa,Kannan NareshBabu,Ramasamy Kim
Reference12 articles.
1. Defective discoidin domain structure, subunit assembly, and endoplasmic reticulum processing of retinoschisin are primary mechanisms responsible for X-linked retinoschisis;Wu;J Biol Chem,2003
2. X-linked juvenile retinoschisis: Clinical diagnosis, genetic analysis, and molecular mechanisms;Molday;Prog Retin Eye Res,2012
3. RS1, a discoidin domain-containing retinal cell adhesion protein associated with X-linked retinoschisis, exists as a novel disulfide-linked octamer;Wu;J Biol Chem,2005
4. Genetic variations in the hotspot region of RS1 gene in Indian patients with juvenile X-linked retinoschisis;Suganthalakshmi;Mol Vis,2007
5. Unusual manifestations of x-linked retinoschisis: Clinical profile and diagnostic evaluation;Shukla;Am J Ophthalmol,2007