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Initial description of the human NLRP3 promoter
Mutations in NLRP3 (CIAS1) are identified in a continuum of related inflammatory disorders, known as cryopyrinopathies since NLRP3 codes for the protein cryopyrin. Approximately 40% of patients with classic presentation lack mutations in the coding region of NLRP3 suggesting heterogeneity or epigene...
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| Foilsithe in: | Genes Immun |
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| Main Authors: | , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2008
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4477692/ https://ncbi.nlm.nih.gov/pubmed/18719602 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gene.2008.66 |
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