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

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