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	21.	A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease). [electronic resource] by Faiyaz-Ul-Haque, M Al-Jefri, A Abalkhail, H A Toulimat, M Al-Muallimi, M A Pulicat, M S Gaafar, A Alaiya, A A Al-Dayel, F Peltekova, I Zaidi, S H E Producer: 20100217 In: Clinical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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