Associated Papers
Three novel mutations in CYBA among 22 Iranians with Chronic granulomatous disease.
Badalzadeh M et al.
International Journal of Immunogenetics, 2017
CYBA encoding p22(phox), the cytochrome b558 alpha polypeptide: gene structure, expression, role and physiopathology.
Stasia MJ
Gene, 2016
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update).
Roos D et al.
Blood Cells, Molecules & Diseases, 2010
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease.
Köker MY et al.
European Journal of Clinical Investigation, 2009
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