A case of concomitant autosomal recessive osteopetrosis and G6PD deficiency.

Autor: Montazeri, Farhad, Montazeri, Ghodrat, Bedayat, Arash, Sedighi, Nahid
Předmět:
Zdroj: Annals of Hematology; Apr2008, Vol. 87 Issue 4, p333-335, 3p, 1 Color Photograph
Abstrakt: A letter to the editor is presented that discusses a case of concomitant autosomal recessive osteopetrosis and glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Databáze: Complementary Index