Less IgA deposits with more severe disease: the immunoclinical paradox in Henoch-Schonlein Purpura with MEFV mutations

Ilgen, UfukNergizoglu, Gokhan2024-06-122024-06-1220190770-31981434-9949https://doi.org/10.1007/s10067-019-04677-0https://hdl.handle.net/20.500.14551/24995[Abstract Not Available]en10.1007/s10067-019-04677-0info:eu-repo/semantics/closedAccessFamilial Mediterranean FeverClassificationNephropathyGeneLess IgA deposits with more severe disease: the immunoclinical paradox in Henoch-Schonlein Purpura with MEFV mutationsLetter381133113313Q3WOS:0004937628000422-s2.0-8506920865131317424Q2