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Antibody deficiency associated with an inherited autosomal dominant mutation in TWEAK

Mutations in the TNF family of proteins have been associated with inherited forms of immune deficiency. Using an array-based sequencing assay, we identified an autosomal-dominant deficiency in TNF-like weak inducer of apoptosis (TWEAK; TNFSF12) in a kindred with recurrent infection and impaired anti...

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Detalhes bibliográficos
Main Authors: Wang, Hong-Ying, Ma, Chi A., Zhao, Yongge, Fan, Xiying, Zhou, Qing, Edmonds, Pamela, Uzel, Gulbu, Oliveira, Joao Bosco, Orange, Jordan, Jain, Ashish
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3612633/
https://ncbi.nlm.nih.gov/pubmed/23493554
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1221211110
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