Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype

Sadeleştirilmiş öğe sayfası
dc.contributor.authorOnen, Merve Ozkilinc
dc.contributor.authorOnat, I, Umut
dc.contributor.authorUgurlu, Serdal
dc.contributor.authorTimucin, Ahmet C.
dc.contributor.authorArslan, Devrim Oz
dc.contributor.authorEverest, Elif
dc.contributor.authorOzdogan, Huri
dc.contributor.authorTuranli, Eda Tahir
dc.date.accessioned2025-10-16T15:15:57Z
dc.date.issued2023
dc.identifier.doi10.1093/rheumatology/kead044
dc.identifier.otherWOS:000927133100001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/6582
dc.publisherOXFORD UNIV PRESS
dc.sourceRHEUMATOLOGY
dc.subjectMEFV\\-negative
dc.subjectFMF
dc.subjectMKD\\-overlapping
dc.subjectPSTPIP1
dc.subjectpyrin
dc.subjectinflammation
dc.titleDetection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype
dc.typeArticle

Dosyalar

Koleksiyonlar

WOS