Isiyel, E; Ezgu, SAB; Caliskan, S; Akman, S; Akil, I; Tabel, Y; Akinci, N; Ozdogan, EB; Ozel, A; Eroglu, FK; Ezgu, FS
(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 ...