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Novel heterozygous C243Y A20/TNFAIP3 gene mutation is responsible for chronic inflammation in autosomal-dominant Behçet's disease

OBJECTIVE: Although Behçet's disease (BD) is a chronic inflammatory disorder of uncertain aetiology, the existence of familial BD with autosomal-dominant traits suggests that a responsibility gene (or genes) exists. We investigated a Japanese family with a history of BD to search for pathogenic...

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Detalhes bibliográficos
Publicado no:RMD Open
Main Authors: Shigemura, Tomonari, Kaneko, Naoe, Kobayashi, Norimoto, Kobayashi, Keiko, Takeuchi, Yusuke, Nakano, Naoko, Masumoto, Junya, Agematsu, Kazunaga
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4860863/
https://ncbi.nlm.nih.gov/pubmed/27175295
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/rmdopen-2015-000223
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