Pediatric Neurology Briefs
Published 2008 | Version v1.0.0
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Idiopathic Infantile Nystagmus, With and Without FRMD7 Gene Mutations

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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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PNB-22-44-a

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Created
2008
When the item was originally created.