Matsuda I, Oka Y, Taniguchi N, Furuyama M, Kodama S, Arashima S, Mitsuyama T
J Pediatr. 1976 Apr;88(4 Pt 1):581-3. doi: 10.1016/s0022-3476(76)80010-8.
A male child with chronic granulomatous disease is described in whom glutathione peroxidase deficiency of leukocytes was identified. Stability and activity of G-6-PD and activity of NADPH oxidase were normal. The leukocytes of the parents showed intermediate activities of glutathione peroxidase, suggesting the possibility of autosomal recessive inheritance.