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

• Hoofdauteurs: Gunter Assmann (Auteur), Michaela Köhm (Auteur), Volker Schuster (Auteur), Frank Behrens (Auteur), Rotraut Mössner (Auteur), Nina Magnolo (Auteur), Vinzenz Oji (Auteur), Harald Burkhardt (Auteur), Ulrike Hüffmeier (Auteur)
• Formaat: Boek
• Gepubliceerd in: BMC, 2020-05-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: 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...