학술논문
Identification of a neutrophil-specific PIK3R1 mutation facilitates targeted treatment in a patient with Sweet syndrome.
Document Type
Journal Article
Author
Bhattacharya, Shreya; Basu, Sayon; Sheng, Emily; Murphy, Christina; Wei, Jenny; Kersh, Anna E.; Nelson, Caroline A.; Bryer, Joshua S.; Ashchyan, Hovik A.; Steele, Katherine; Forrestel, Amy; Seykora, John T.; Micheletti, Robert G.; James, William D.; Rosenbach, Misha; Leung, Thomas H.; Murphy, Christina M; Steele, Katherine T; Forrestel, Amy K
Source
Subject
*SWEET'S syndrome
*SOMATIC mutation
*PYODERMA gangrenosum
*GAIN-of-function mutations
*PI3K/AKT pathway
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Language
ISSN
0021-9738
Abstract