Hematologically important mutations: X-linked chronic granulomatous disease (fourth update)

D Roos, K Van Leeuwen, AP Hsu, DL Priel… - Blood Cells, Molecules …, 2021 - Elsevier
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in
250,000 individuals. CGD patients suffer from severe bacterial and fungal infections. The …

Hematologically important mutations: X-linked chronic granulomatous disease (third update)

D Roos, DB Kuhns, A Maddalena, J Roesler… - Blood Cells, Molecules …, 2010 - Elsevier
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in
250,000 individuals. The disease is caused by a lack of superoxide production by the …

Hematologically important mutations: X-linked chronic granulomatous disease (second update)

PG Heyworth, JT Curnutte, J Rae, D Noack… - Blood Cells, Molecules …, 2001 - Elsevier
The most common form of chronic granulomatous disease (CGD) is caused by mutations in
the X-linked gene (CYBB, located at Xp21. 1) for the protein gp91phox. This protein is one of …

Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update)

D Roos, K Van Leeuwen, AP Hsu, DL Priel… - Blood Cells, Molecules …, 2021 - Elsevier
Chronic granulomatous disease (CGD) is an immunodeficiency disorder affecting about 1 in
250,000 individuals. CGD patients suffer from severe, recurrent bacterial and fungal …

Molecular diagnosis of X-linked chronic granulomatous disease in Iran

S Teimourian, Z Rezvani, M Badalzadeh… - International journal of …, 2008 - Springer
Chronic granulomatous disease (CGD) is an inherited disorder of pathogen killing by
phagocytic leukocytes caused by mutations in NADPH oxidase subunits. Patients with CGD …

[引用][C] Hematologically important mutations: X-linked chronic granulomatous disease—an update

PG Heyworth, JT Curnutte, J Rae, D Noack… - Blood Cells, Molecules …, 1997 - Elsevier
The most common form of chronic granulomatous disease (CGD) is caused by mutations in
the X-linked gene (CYBB, located at Xp21. 1) for the protein gp91-phox. This protein is one …

[引用][C] Hematologically important mutations: X-linked chronic granulomatous disease

AR Cross, JT Curnutte, J Rae, PG Heyworth - Blood Cells, Molecules, and …, 1996 - Elsevier
The most common form of chronic table will list the mutations causing the autosomal
granulomatous disease (CGD) is caused by recessive forms of CGD. mutations in the X …

Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)

D Roos, DB Kuhns, A Maddalena, J Bustamante… - Blood Cells, Molecules …, 2010 - Elsevier
Chronic granulomatous Disease (CGD) is an immunodeficiency disorder affecting about 1 in
250,000 individuals. The disease is caused by mutations in the genes encoding the …

Molecular characterization of a large cohort of patients with chronic granulomatous disease and identification of novel CYBB mutations: an Italian multicenter study

G Di Matteo, L Giordani, A Finocchi, A Ventura… - Molecular …, 2009 - Elsevier
Chronic Granulomatous Disease (CGD) is a rare inherited disorder in which phagocytes fail
to produce antimicrobial superoxide because NADPH oxidase activity is absent. In about …

[HTML][HTML] Characterization of 17 new cases of X-linked chronic granulomatous disease with seven novel mutations in the CYBB gene

H von Goessel, JP Hossle, R Seger, T Gungor - Experimental hematology, 2006 - Elsevier
OBJECTIVE: Molecular identification and clinical characterization of genetic mutations in
patients with X-linked chronic granulomatous disease (CGD). PATIENTS AND METHODS …