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A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease)

✍ Scribed by M Faiyaz-Ul-Haque; A Al-Jefri; HA Abalkhail; M Toulimat; MA Al-Muallimi; MS Pulicat; A Gaafar; AA Alaiya; F Al-Dayel; I Peltekova; SHE Zaidi

Book ID: 110888857
Publisher: John Wiley and Sons
Year: 2009
Tongue: English
Weight: 513 KB
Volume: 76
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2009.01244.x

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