Welcome to Prism!

Upload scholarly work, create communities, get citable links and more. To get the most out of Prism, log in with your NetID and check out our guide.

Published 2008 | Version v1.0.0
Journal Article Open

Idiopathic Infantile Nystagmus, With and Without FRMD7 Gene Mutations

Abstract

Clinical features and eye movement recordings of 90 subjects with mutations in the gene (FRMD7 group) were compared to 48 without mutations non-FRMD7 group) but with clinical idiopathic infantile nystagmus (IIN), in a study at University of Leicester, Leicester Royal Infirmary, Leeds General Infirmary, Royal Preston Hospital, Addenbrooks Hospital, Cambridge, UK; Wills Eye Hospital, Philadelphia, USA; and Medical University Graz, Austria.

Files

PNB-22-44-a.pdf
Files (1.4 MB)
Name Size Download all
md5:4b73092a2dee1915906e64600175cab1
1.4 MB Preview Download

Additional details

Created:
March 30, 2023
Modified:
March 30, 2023