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Figure 1 | BMC Gastroenterology

Figure 1

From: Neonatal intrahepatic cholestasis caused by citrin deficiency: prevalence and SLC25A13mutations among thai infants

Figure 1

Agraose gel electrophoresis showing IVS16ins3kb (XIX), Mutations 851del4 (I), and p.M1? variant. A: 1.5% gel revealing 3.65 kb fragment representing the IVS16ins3kb (XIX) and the 990bp fragment representing normal allele.; B: 1.5% gel showing exon 9-PCR-HpyCH4IV restriction digest. The 851del4 mutation abolishes the restriction site, whereas the normal allele was cut, yielding 179 and 122bp fragments.; C: 2.5% gel showing 109bp-product of PCR using primers E1F/E1_1MT-R. The p.M1? allele produces an EagI restriction site, yielding 89 and 20bp-fragments.

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