Idiopathic Infantile Nystagmus, With and Without FRMD7 Gene Mutations
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 Infirma...
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| Format: | Article |
| Language: | English |
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Pediatric Neurology Briefs Publishers
2008-06-01
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| Series: | Pediatric Neurology Briefs |
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| Online Access: | https://www.pediatricneurologybriefs.com/articles/899 |