Fig. 3From: Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human geneMutational profile of the IVS3 -5delGCAA deletion located at the intron3-exon4 of the C10orf71 gene in the two heterozygous normal parents (III7 and III8) and their two affected homozygous children (IV10 and IV11)Back to article page