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.

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