Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease - Prototype for a structurally novel flavoenzyme family

Author: Roesler J.   Heyden S.   Burdelski M.   Schafer H.   Kreth H.-W.   Lehmann R.   Paul D.   Marzahn J.   Gahr M.   Rosen-Wolff A.  

Publisher: Elsevier

ISSN: 0301-472X

Source: Experimental Hematology, Vol.27, Iss.3, 1999-03, pp. : 505-511

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Abstract