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Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase
- Roos, D (author)
- de Boer, M (author)
- Koker, MY (author)
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- Dekker, J (author)
- Singh-Gupta, V (author)
- Sanal, O (author)
- Kurenko-Deptuch, M (author)
- Jolles, S (author)
- Wolach, B (author)
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- (creator_code:org_t)
- Hindawi Limited, 2006
- 2006
- English.
- In: Human mutation. - : Hindawi Limited. - 1098-1004 .- 1059-7794. ; 27:12, s. 1218-1229
- Journal article (peer-reviewed)
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- Roos, D
- de Boer, M
- Koker, MY
- Dekker, J
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- Palmblad, J
- Sanal, O
- Kurenko-Deptuch, ...
- Jolles, S
- Wolach, B
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- Human mutation
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- Karolinska Institutet
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