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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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Bibliografische gegevens
Gepubliceerd in:Clin Case Rep
Hoofdauteurs: Degrugillier, Fanny, Simon, Stéphanie, Aissat, Abdel, Remus, Natascha, Mekki, Chadia, Decrouy, Xavier, Hatton, Aurélie, Hinzpeter, Alexandre, Hoffmann, Brice, Sermet‐Gaudelus, Isabelle, Callebaut, Isabelle, Fanen, Pascale, Prulière‐Escabasse, Virginie
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: John Wiley and Sons Inc. 2019
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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