Mutational analysis of AGXT gene in Libyan children with primary hyperoxaluria type 1 at Tripoli Children Hospital
. . Rhuma NR, Fituri OA, Sabei LT. . Saudi J Kidney Dis Transpl. 2018 Jan-Feb;29(1):30-38. doi: 10.4103/1319-2442.225202. Abstract Primary hyperoxaluria type 1 (PH1) is an inborn error of glyoxylate metabolism. It results from genetic mutation of the AGXT gene. The study objective was to verify the clinical and epidemiological patterns of PH1 in Libyan …