- Tytuł:
- Identification of a neutrophil-specific PIK3R1 mutation facilitates targeted treatment in a patient with Sweet syndrome.
- Autorzy:
- Temat:
-
NATIONAL Institutes of Health (U.S.)
SWEET'S syndrome
SOMATIC mutation
PYODERMA gangrenosum
GAIN-of-function mutations
PI3K/AKT pathway - Źródło:
- Journal of Clinical Investigation. 1/3/2023, Vol. 133 Issue 1, p1-8. 8p.
Czasopismo naukowe