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RIG-I-Like Receptor Signaling in Singleton-Merten Syndrome

Singleton-Merten syndrome (SMS) is an autosomal dominant, multi-system innate immune disorder characterized by early and severe aortic and valvular calcification, dental and skeletal abnormalities, psoriasis, glaucoma, and other varying clinical findings. Recently we identified a specific gain-of-fu...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Lu, Changming, MacDougall, Mary
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5600918/
https://ncbi.nlm.nih.gov/pubmed/28955379
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2017.00118
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