Homozygous HAX1 mutations in severe congenital neutropenia patients with sporadic disease: a novel mutation in two unrelated British kindreds

✍ Scribed by Bradley N. Smith; Phil J. Ancliff; Arnold Pizzey; Asim Khwaja; David C. Linch; Rosemary E. Gale

• Book ID: 108676102
• Publisher: John Wiley and Sons
• Year: 2009
• Tongue: English
• Weight: 251 KB
• Volume: 144
• Category: Article
• ISSN: 0007-1048
• DOI: 10.1111/j.1365-2141.2008.07493.x