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-Reference-Cited by-同舟云学术

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

Published:2003-12 Issue:3 Volume:109 Page:308-317
ISSN:1521-6616
Container-title:Clinical Immunology
language:en
Short-container-title:Clinical Immunology

Author:

Anderson-Cohen Mindy,Holland Steve M,Kuhns Doug B,Fleisher Thomas A,Ding Li,Brenner Sebastian,Malech Harry L,Roesler Joachim

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference59 articles.

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5. Molecular basis of chronic granulomatous disease;Smith;Blood,1991

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