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. 2019 Feb 22;11(2):461. doi: 10.3390/nu11020461

Figure 2.

Figure 2

Schematic presentation of mutations in congenital lactase deficiency (CLD) and their location in the exons of the gene of lactase-phlorizin hydrolase (LPH). I-IV correspond to the four homologous domains of pro-LPH (see references [17,23,36,37]).