
Keywords: آلانین گلیکسیلات آمینوترانسفراز; PH1; Primary hyperoxaluria type 1; AGT; alanine glyoxylate aminotransferase; vitamin B6; pyridoxine; CaOx; calcium oxalate; NC; nephrocalcinosis; ESRD; end-stage renal disease; AGT-Mi; minor allele haplotype; HGMD; Human Gene Mutation Database; SNPs; sing