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Muckle–Wells syndrome in an Indian family associated with NLRP3 mutation
Muckle — Wells syndrome (MWS) is a rare autosomal dominant disease that belongs to a group of hereditary periodic fever syndromes. It is part of the wider spectrum of the cryopyrin-associated periodic syndrome (CAPS) which has only rarely been described in non-Caucasian individuals. It is characteri...
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| Publicado no: | J Postgrad Med |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4943435/ https://ncbi.nlm.nih.gov/pubmed/25766347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0022-3859.153107 |
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