Article Text

Download PDFPDF

Complex mutations of USH2A gene denote ARRP

Statistics from Altmetric.com

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. …

View Full Text

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.