Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient.

Bonizzato, A

Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient. [electronic resource] - Biochemical and biophysical research communications Feb 1997 - 861-3 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

0006-291X

10.1006/bbrc.1997.6204 doi


Genes
Granulomatous Disease, Chronic--genetics
Humans
Neutrophils--physiology
Phosphoproteins--genetics
Point Mutation
Polymerase Chain Reaction
Polymorphism, Single-Stranded Conformational