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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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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
National Academy of Sciences
2013
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| Assuntos: | |
| 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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