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Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia
BACKGROUND: Familial Mediterranean fever (FMF), an autosomal recessive, autoinflammatory disease that is common in Arabs, Jews, Armenians and Turks, is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The disease is characterised by recurrent fever, peritonitis, pleuritis,...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Ann Saudi Med |
|---|---|
| Prif Awduron: | , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
King Faisal Specialist Hospital and Research Centre
2019
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6894460/ https://ncbi.nlm.nih.gov/pubmed/31804137 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5144/0256-4947.2019.382 |
| Tagiau: |
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