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Fig. 5 | Journal of Medical Case Reports

Fig. 5

From: Novel compound heterozygote mutations in the ATP7B gene in an Iranian family with Wilson disease: a case report

Fig. 5

Picture of 2% agarose gel electrophoresis of amplification-refractory mutation system test products for exon 18 variant (c.3809A>G). Well 1: negative polymerase chain reaction test control (no template control; NTC). Well 2: normal case homozygote for AA. Well 3: IV:5 member in the family who was heterozygote for c.3809A>G (AG). Well 4–11: eight healthy members. Well 12: 100 kb ladder

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