Mastocytosis associated with a rare germline KIT K509I mutation displays a well-differentiated mast cell phenotype

BACKGROUND: Mastocytosis associated with germline KIT activating mutations is exceedingly rare. We report the unique clinicopathologic features of a patient with systemic mastocytosis caused by a de novo germline KIT K509I mutation. OBJECTIVES: To investigate the impact of the germline KIT K509I mut...

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Detaylı Bibliyografya
Asıl Yazarlar: Chan, Eunice Ching, Bai, Yun, Kirshenbaum, Arnold. S., Fischer, Elizabeth R., Simakova, Olga, Bandara, Geethani, Scott, Linda M., Wisch, Laura B., Cantave, Daly, Carter, Melody C., Lewis, John C., Noel, Pierre, Maric, Irina, Gilfillan, Alasdair M., Metcalfe, Dean D., Wilson, Todd M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2014
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4125511/
https://ncbi.nlm.nih.gov/pubmed/24582309
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2013.12.1090
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