Genotype-phenotype studies in infantile nystagmus with emphasis on the novel Frmd7 gene
FRMD7 mutations are a major cause of idiopathic infantile nystagmus (IIN). Infantile nystagmus can also be associated with albinism, PAX6 mutations and achromatopsia; these disorders are associated with afferent visual anomalies which pose the question could this be a common aetiological factor for...
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University of Leicester
2012
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| Online Access: | http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.554064 |