Effective treatment of TNFα inhibitors in Chinese patients with Blau syndrome

OBJECTIVES: Blau syndrome (BS) is a rare dominantly inherited autoinflammatory disorder associated with mutations in the nucleotide-binding oligomerization domain containing 2 (NOD2) gene. Biologic therapy of BS yielded diverse results. We aimed to evaluate clinical features and outcomes of Chinese...

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Detalles Bibliográficos
Autores principales: Chen, Jing, Luo, Yi, Zhao, Mengzhu, Wu, Di, Yang, Yunjiao, Zhang, Wen, Shen, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852754/
https://www.ncbi.nlm.nih.gov/pubmed/31718710
http://dx.doi.org/10.1186/s13075-019-2017-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6852754/
https://www.ncbi.nlm.nih.gov/pubmed/31718710
http://dx.doi.org/10.1186/s13075-019-2017-5

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