Associated Papers
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).
Roos D et al.
Blood Cells, Molecules & Diseases, 2010
Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations.
Köker MY et al.
European Journal of Clinical Investigation, 2009
Genetics and immunopathology of chronic granulomatous disease.
Stasia MJ et al.
Seminars in Immunopathology, 2008
Molecular and functional characterization of a new X-linked chronic granulomatous disease variant (X91+) case with a double missense mutation in the cytosolic gp91phox C-terminal tail.
Stasia MJ et al.
Biochimica Et Biophysica Acta, 2002
The active N-terminal region of p67phox. Structure at 1.8 A resolution and biochemical characterizations of the A128V mutant implicated in chronic granulomatous disease.
Grizot S et al.
The Journal of Biological Chemistry, 2001
[The NADPH-oxidase complex in chronic granulomatous disease: preliminary description of a cluster in Mérida-Venezuela].
Salmen S et al.
Investigacion Clinica, 1999
Identification of a double mutation (D160V-K161E) in the p67phox gene of a chronic granulomatous disease patient.
Bonizzato A et al.
Biochemical and Biophysical Research Communications, 1997
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