p67-phox deficient chronic granulomatous disease due to heterozygous defects in exons 4 and 12 of the NCF-2 gene

Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations

“…4). This mutation was previously described in heterozygous form by Khan et al [23] and in homozygous form by Patino et al [24] and Wolach et al [11].…”