Isiyel, E.; Ezgu, S.A.B.; Caliskan, S.; Akman, S.; Akil, I.; Tabel, Y.; Akinci, N.; Ozdogan, E.B.; Ozel, A.; Eroglu, F.K.; Ezgu, F.S.
(2016)
Primary hyperoxaluria type 1 (PH1) is a rare, autosomal recessive disease, caused by the defect of AGXT gene encoding hepatic peroxisomal alanine glyoxylateaminotransferase (AGT). This enzyme is responsible for the conversion ...