G. Celik; Şen, Şaduman; Sipahi, Savaş; C. Akkin; S. Tamsel; H. Toz; C. Hoscoskun
(INFORMA HEALTHCARE, 2010)
Primary hyperoxaluria (PH) is a rare autosomal recessive disease caused by the functional defect of alanine-glyoxylate aminotransferase (AGT) enzyme in the liver and it is characterized by the deposition of diffuse calcium ...