TY - JOUR T1 - Complex mutations of USH2A gene denote ARRP JF - British Journal of Ophthalmology JO - Br J Ophthalmol SP - 1125 LP - 1125 DO - 10.1136/bjo.87.9.1125 VL - 87 IS - 9 A2 - , Y1 - 2003/09/01 UR - http://bjo.bmj.com/content/87/9/1125.abstract N2 - A study of mutations associated with non-syndromic autosomal recessive retinitis pigmentosa (ARRP) in Spanish patients will ultimately help our knowledge of events leading to blindness or deafness, or both. Before then, though, the complexities of ARRP phenotypes and how these relate to genetic make up will take some unravelling. … ER -