CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model

Related Research Area: 
Gene Therapy Lab
Citation: 
Wert KJ, Bassuk AG, Wu W-H, et al. "CAPN5 mutation in hereditary uveitis: the R243L mutation increases calpain catalytic activity and triggers intraocular inflammation in a mouse model." Human molecular genetics. 2015;24:4584-4598.
Year of Publication: 
2015