PurposeRPGR is the most common cause of X-linked retinitis pigmentosa (RP), of which female carriers are also frequently affected. The aim of the current study was to explore the RPGR variation spectr
Purpose: To report novel variants in IFT140 and IFT172 genes in three patients with similar retinal dystrophy phenotypes. Methods: This is a case series of two brothers with known retinal dystrophy, r
