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

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

• Book ID: 116366075
• Publisher: Elsevier Science
• Year: 2003
• Tongue: English
• Weight: 508 KB
• Volume: 109
• Category: Article
• ISSN: 1090-2341
• DOI: 10.1016/j.clim.2003.08.002