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Fig. 6 | Human Genomics

Fig. 6

From: Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene

Fig. 6

C10orf71 gene PCR product. A the size of the amplicon (379 bp) in various fetal tissues, and leukocytes (blood) of unrelated control individual. B Polyacrylamide gel of the cDNA amplicon generated and amplified by RT-PCR showing the normal size of the amplicon for the positive control (379 bp) and for two affected patients IV10 and IV11 (383 bp)

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