Article
Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG.
Documenta ophthalmologica. Advances in ophthalmology - 1 Jan 1999
Bradshaw K, George N, Moore A, Trump D
Abstract excerpt
Intensity-series rod and cone ERGs were recorded in 19 patients with XLRS and 26 control eyes. All patients were examined by one ophthalmologist and diagnosed on the basis of fundus appearance and evidence of the disease in other males in the same family. Mutations in the XLRS1 gene have been identified in 15 of the patients. Dark-adapted ERGs were significantly different from controls for all test conditions and...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
