Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleComment on: Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype.AuthorsZervou, Maria I; Goulielmos, George NSubjectsGENETIC mutation; RHEUMATOLOGY; WESTERN immunoblotting; PRECIPITIN tests; APOPTOSIS; MEVALONATE kinase deficiency; PYODERMA gangrenosum; AUTOINFLAMMATORY diseases; PHENOTYPESPublicationRheumatology, 2023, Vol 62, Issue 9, pe280ISSN1462-0324Publication typeLetter to the EditorDOI10.1093/rheumatology/kead102