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Fig. 4 | Journal of Medical Case Reports

Fig. 4

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

Fig. 4

Picture of 2% agarose gel electrophoresis of amplification-refractory mutation system test products for exon 6 variant (c.1924G>C). Well 1: negative polymerase chain reaction test control (no template control; NTC). Well 2: normal case homozygote for GG. Well 3: IV:5 member in the family who was heterozygote for c.1924G>C (GC). Well 4–11: eight healthy members. Well 12: 100 kb ladder

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Journal of Medical Case Reports

ISSN: 1752-1947