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Blau Syndrome, the prototypic auto-inflammatory granulomatous disease

Blau syndrome is a monogenic disease resulting from mutations in the pattern recognition receptor NOD2, and is phenotypically characterized by the triad of granulomatous polyarthritis, dermatitis and uveitis. This paper reviews briefly the classical clinical features of the disease, as well as more...

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Detalhes bibliográficos
Main Authors: Wouters, Carine H, Maes, Anne, Foley, Kevin P, Bertin, John, Rose, Carlos D
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4136643/
https://ncbi.nlm.nih.gov/pubmed/25136265
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1546-0096-12-33
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