A novel clinical syndrome associating severe congenital neutropenia and complex development aberrations caused by deficiency of G6PC3 (ESID Plenary Session VI: Novel Primary Immunodeficiencies and Late breakers)

✍ Scribed by K. Boztug

• Book ID: 117422927
• Publisher: Elsevier Science
• Year: 2009
• Tongue: French
• Weight: 130 KB
• Volume: 30
• Category: Article
• ISSN: 0248-8663
• DOI: 10.1016/s0248-8663(09)72097-1