LLNI Funded Publications
A novel L218P mutation in NADH-cytochrome b5 reductase associated with type I recessive congenital methemoglobinemia.
Author:Arikoglu T
Other Authors: Yarali N, Kara A, Bay A, Bozkaya IO, Tunc B, Percy MJ,
Journal:Pediatr Hematol Oncol
Date: 2009
