Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia

✍ Scribed by Göran Carlsson; Malin Melin; Niklas Dahl; Kim Göransdotter Ramme; Magnus Nordenskjöld; Jan Palmblad; Jan-Inge Henter; Bengt Fadeel

• Book ID: 114815087
• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 386 KB
• Volume: 96
• Category: Article
• ISSN: 0803-5253
• DOI: 10.1111/j.1651-2227.2007.00274.x