Rare C1q deficiency presenting as pediatric SLE: A case study of two consanguineous siblings

Sadeleştirilmiş öğe sayfası
dc.contributor.authorParlar, Kerem
dc.contributor.authorAktas, Berkay
dc.contributor.authorSicakyuz, Sena Ladin
dc.contributor.authorSahin, Sezgin
dc.contributor.authorKasapcopur, Ozgur
dc.contributor.authorUgurlu, Serdal
dc.date.accessioned2025-10-16T15:11:52Z
dc.date.issued2025
dc.identifier.doi10.1016/j.reuma.2025.501843
dc.identifier.otherWOS:001463286400001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5081
dc.publisherELSEVIER ESPANA SLU
dc.sourceREUMATOLOGIA CLINICA
dc.subjectC1q deficiency
dc.subjectSystemic lupus erythematosus
dc.subjectNeuropsychiatric involvement
dc.subjectChillblain lesions
dc.titleRare C1q deficiency presenting as pediatric SLE: A case study of two consanguineous siblings
dc.typeArticle

Dosyalar

Koleksiyonlar

WOS