- Title
- A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease)
- Creators - without role
- M. Faiyaz-Ul-Haquea - College Station Medical CenterA. Al-Jefric - King Faisal Specialist Hosp & Res Ctr, Dept Pediat Hematol Oncol, Riyadh 11211, Saudi ArabiaH. A. Abalkhail - King Faisal Specialist Hospital & Research CentreM. Toulimat - King Faisal Specialist Hospital & Research CentreM. A. Al-Muallimi - King Faisal Specialist Hospital & Research CentreM. S. Pulicat - King Faisal Specialist Hospital & Research CentreA. Gaafar - King Faisal Specialist Hospital & Research CentreA. A. Alaiya - King Faisal Specialist Hospital & Research CentreF. Al-Dayel - King Faisal Specialist Hospital & Research CentreI. Peltekova - Queen's UniversityS. H. E. Zaidi - College Station Medical Center
- Publication Details
- Clinical genetics, Vol.76(6), pp.569-572
- Publisher
- Wiley
- Number of pages
- 4
- Identifiers
- 9913862508331
- Academic Unit
- King Faisal University; Alfaisal University; King Saud Bin Abdulaziz University for Health Sciences
- Language
- English
- Resource Type
- Journal article
Journal article
A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease)
Clinical genetics, Vol.76(6), pp.569-572
01/12/2009
PMID: 19796188
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