Authors: NAUSEEF WM COGLEY M BOCK S PETRIDES PE

Citation: Wm. Nauseef et al., PATTERN OF INHERITANCE IN HEREDITARY MYELOPEROXIDASE DEFICIENCY ASSOCIATED WITH THE R569W MISSENSE MUTATION, Journal of leukocyte biology, 63(2), 1998, pp. 264-269

Authors: SMOLEN JE HESSLER RJ NAUSEEF WM COGLEY M JOE Y

Citation: Je. Smolen et al., IDENTIFICATION AND CLONING OF THE FUSION PROTEIN VAMP-2 IN HL-60 CELLS AND HUMAN NEUTROPHILS, Molecular biology of the cell, 8, 1997, pp. 1713-1713

Authors: PETRIDES PE BOCK S COGLEY M NAUSEEF WM

Citation: Pe. Petrides et al., COMPOUND HETEROZYGOSITY IN GENETIC MYELOPEROXIDASE DEFICIENCY ASSOCIATED WITH THE R569W MUTATION, Blood, 90(10), 1997, pp. 2909-2909

Authors: NAUSEEF WM COGLEY M MCCORMICK S

Citation: Wm. Nauseef et al., EFFECT OF THE R569W MISSENSE MUTATION ON THE BIOSYNTHESIS OF MYELOPEROXIDASE, The Journal of biological chemistry, 271(16), 1996, pp. 9546-9549

Authors: NAUSEEF WM BRIGHAM S COGLEY M

Citation: Wm. Nauseef et al., HEREDITARY MYELOPEROXIDASE DEFICIENCY DUE TO A MISSENSE MUTATION OF ARGININE-569 TO TRYPTOPHAN, The Journal of biological chemistry, 269(2), 1994, pp. 1212-1216