A novel missense mutation in the HAX1 gene in severe congenital neutropenia patients (Kostmann disease)期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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

Authors:	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

Affiliation:	1. Department of Pathology and Laboratory Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia;2. College of Medicine, Alfaisal University, Riyadh, Saudi Arabia;3. Department of Pediatric Hematology/Oncology;4. Department of Biological and Medical Research, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia;5. Department of Medicine, Queen's University, Kingston, Ontario, Canada;6. Department of Medicine, University Health Network and University of Toronto, Ontario, Canada

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