Duo Sun

Mouse models of X-linked juvenile retinoschisis have an early onset phenotype, the severity of which varies with genotype.

Hong Li, B. Sagdullaev, B. Bell, 2019, Human Molecular Genetics.

Retinoschisin deficiency induces persistent aberrant waves of activity affecting neuroglial signaling in the retina

J. J. McAnany, Julia C. Batoki, B. Sagdullaev, 2021, bioRxiv.

Wild Type and Mutant Retinoschisin Subunits Co-assemble When Expressed in the Same Cells

W. Olson, Jifang Tao, C. Romano, 2018 .