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Fig. 2 | BMC Nephrology

Fig. 2

From: Identification of compound heterozygous patients with primary hyperoxaluria type 1: clinical evaluations and in silico investigations

Fig. 2

a Sequence chromatograms showing the presence of c.32C > T, c.731 T > C and c.1020A > G variants in Family F1. b Multiple sequence alignment of alanine:glyoxylate aminotransferase (AGT) with different species showing the aminoacids at position 11, 244 and 340. The concerned amino acids are boxed. c Model of AGT-LTM variant obtained by Deep View/Suiss-PDB viewer 3.7 software showing the aminoacids at position 11, 244 and 340. d A schematic drawing of the AGT domains showing the aminoacids at position 11, 244 and 340

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BMC Nephrology

ISSN: 1471-2369

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