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Hyper-IgD syndrome/mevalonate kinase deficiency: what is new?
Mevalonate kinase deficiency or hyper-IgD syndrome is a hereditary autoinflammatory syndrome caused by mutations in the mevalonate kinase gene. In this review, we will discuss new findings in this disorder that have been published in the last 2 years. This includes new insights into pathophysiology,...
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| Publicado no: | Semin Immunopathol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4491100/ https://ncbi.nlm.nih.gov/pubmed/25990874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00281-015-0492-6 |
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