Comparative analysis of mutation of tyrosine kinase kit in mast cells from patients with systemic mast cell activation syndrome and healthy subjects
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Immunology
Link
http://link.springer.com/content/pdf/10.1007/s00251-010-0474-8.pdf
Reference36 articles.
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2. Alvarez-Twose I, González de Olano D, Sánchez-Muñoz L et al (2010) Clinical, biological, and molecular characteristics of clonal mast cell disorders presenting with systemic mast cell activation symptoms. J Allergy Clin Immunol 125:1269–1278
3. Bandi SR, Brandts C, Rensinghoff M et al (2009) E3 ligase-defective Cbl mutants lead to a generalized mastocytosis and a myeloproliferative disease. Blood 114:4197–4208
4. Bodemer C, Hermine O, Palmérini F et al (2010) Pediatric mastocytosis is a clonal disease associated with D(816)V and other activating c-KIT mutations. J Invest Dermatol 130:804–815
5. Castells M, Austen KF (2002) Mastocytosis: mediator related signs and symptoms. Int Arch Allergy Immunol 127:147–152
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