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Fig. 2 | BMC Gastroenterology

Fig. 2

From: A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe

Fig. 2

Novel mutation of the LCT gene. Results of DNA sequencing of a PCR product containing exon 8 of the LCT gene. Presented are chromatographs of the patient, both parents, and a control. Depicted is the region of codon 1150 demonstrating homozygosity for a 1-bp deletion in the patient. Both parents show a heterozygous pattern for this mutation. wt, wild-type sequence; mut, mutated sequence

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