Mutational analysis of patients with p47-phox-deficient chronic granulomatous disease - The significance of recombination events between the p47-phox gene (NCF1) and its highly homologous pseudogenes

Author: Vazquez N.   Lehrnbecher T.   Chen R.   Christensen B.L.   Gallin J.I.   Malech H.   Holland S.   Zhu S.   Chanock S.J.  

Publisher: Elsevier

ISSN: 0301-472X

Source: Experimental Hematology, Vol.29, Iss.2, 2001-02, pp. : 234-243

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