Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation

Author： Anderson-Cohen M.   Holland S.M.   Kuhns D.B.   Fleisher T.A.   Ding L.   Brenner S.   Malech H.L.   Roesler J.  

Publisher： Elsevier

ISSN： 1521-6616

Source： Clinical Immunology, Vol.109, Iss.3, 2003-12, pp. : 308-317

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