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Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping
Severe chronic rhinosinusitis in children should alert clinicians and extensive CFTR genotyping should be performed. We propose that thorough clinical and functional assessment in severe chronic rhinosinusitis is valuable to discover rare mutations which could be treated by CFTR correctors to postpo...
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| Gepubliceerd in: | Clin Case Rep |
|---|---|
| Hoofdauteurs: | , , , , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
John Wiley and Sons Inc.
2019
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6878083/ https://ncbi.nlm.nih.gov/pubmed/31788264 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.2443 |
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