Mutations in the ELANE Gene are Associated with Development of Periodontitis in Patients with Severe Congenital Neutropenia-Reference-Cited by-同舟云学术

Mutations in the ELANE Gene are Associated with Development of Periodontitis in Patients with Severe Congenital Neutropenia

Published:2011-07-29 Issue:6 Volume:31 Page:936-945
ISSN:0271-9142
Container-title:Journal of Clinical Immunology
language:en
Short-container-title:J Clin Immunol

Author:

Ye Ying,Carlsson Göran,Wondimu Biniyam,Fahlén Annika,Karlsson-Sjöberg Jenny,Andersson Mats,Engstrand Lars,Yucel-Lindberg Tülay,Modéer Thomas,Pütsep Katrin

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy

Link

http://www.springerlink.com/index/pdf/10.1007/s10875-011-9572-0

Reference61 articles.

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2. Kostman R. Infantile genetic agranulocytosis. A review with presentation of ten new cases. Acta Paediatr Scand. 1975;64:362–8.

3. Zeidler C, Germeshausen M, Klein C, Welte K. Clinical implications of ELA2-, HAX1-, and G-CSF-receptor (CSF3R) mutations in severe congenital neutropenia. Br J Haematol. 2009;144:459–67.

4. Boztug K, Klein C. Novel genetic etiologies of severe congenital neutropenia. Curr Opin Immunol. 2009;21:472–80.

5. Dale DC, Bolyard AA, Schwinzer BG, Pracht G, Bonilla MA, Boxer L, et al. The Severe Chronic Neutropenia International Registry: 10-year follow-up report. Support Cancer Ther. 2006;3:220–31.

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