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Familial Mediterranean fever without MEFV mutations: a case–control study
BACKGROUND: Although familial Mediterranean fever (FMF) was originally defined as an autosomal recessive disorder, approximately 10–20% of FMF patients do not carry any FMF gene (MEFV) mutations. Fine phenotype characterization may facilitate the elucidation of the genetic background of the so calle...
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| Gepubliceerd in: | Orphanet J Rare Dis |
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| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2015
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4377009/ https://ncbi.nlm.nih.gov/pubmed/25887307 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-015-0252-7 |
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