Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups

• Asıl Yazarlar: Gunter Assmann (Yazar), Michaela Köhm (Yazar), Volker Schuster (Yazar), Frank Behrens (Yazar), Rotraut Mössner (Yazar), Nina Magnolo (Yazar), Vinzenz Oji (Yazar), Harald Burkhardt (Yazar), Ulrike Hüffmeier (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: BMC, 2020-05-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Abstract Background Syndrome of synovitis acne pustulosis hyperostosis osteitis (SAPHO) and chronic recurrent multifocal osteomyelitis (CRMO) present two diseases of a dermatologic and rheumatologic spectrum that are variable in manifestation und therapeutic response. Genetic risk factors have long...