V Pelletier, M Jambou, N Delphin, E Zinovieva … - Human mutation, 2007 - interscience.wiley.com X-linked forms of retinitis pigmentosa (RP) (XLRP) account for 10 to 20% of
families with RP and are mainly accounted for by mutations in the RP2 or RP
GTPase regulator (RPGR) genes. We report the screening of these genes in a ... Cited by 25 - Related articles - BL Direct - All 3 versions
- ►iovs.org AV Cideciyan, M Swider, TS Aleman, A … - Investigative ophthalmology & visual science, 2005 - ARVO RESULTS. AF images ranged from normal, to spatially homogenous abnormal increase
of intensity, to a spatially heterogenous speckled pattern, to variably sized
patches of low intensity. A parapapillary ring of normal-appearing AF was ... Cited by 20 - Related articles - BL Direct - All 7 versions
C Kannabiran - Expert Review of Ophthalmology, 2008 - ingentaconnect.com Retinitis pigmentosa is a clinically and genetically heterogeneous group of
primary retinal degenerations with autosomal, X-linked and mitochondrial modes
of inheritance. A total of 40 genes have been identified to date that, when ... Cited by 2 - Related articles - All 8 versions