Tabel, Yilmaz
(Academıc press ınc elsevıer scıence, 525 b st, ste 1900, san dıego, ca 92101-4495 usa, 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 ...