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

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 been ass...

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Publicado en:BMC Med Genet
Main Authors: Assmann, Gunter, Köhm, Michaela, Schuster, Volker, Behrens, Frank, Mössner, Rotraut, Magnolo, Nina, Oji, Vinzenz, Burkhardt, Harald, Hüffmeier, Ulrike
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2020
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7216525/
https://ncbi.nlm.nih.gov/pubmed/32397996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01037-7
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