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HAX1 deficiency causes autosomal recessive severe congenital neutropenia (Kostmann disease)

✍ Scribed by Klein, Christoph; Grudzien, Magda; Appaswamy, Giridharan; Germeshausen, Manuela; Sandrock, Inga; Schäffer, Alejandro A; Rathinam, Chozhavendan; Boztug, Kaan; Schwinzer, Beate; Rezaei, Nima

Book ID: 109919486
Publisher: Nature Publishing Group
Year: 2006
Tongue: English
Weight: 544 KB
Volume: 39
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng1940

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