Lataa...
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...
Tallennettuna:
| Julkaisussa: | J Postgrad Med |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2015
|
| Aiheet: | |
| Linkit: | 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 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|