ΔF508

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31	Am. J. Hum. Genet. 51:[removed], 1992 Screening for Five Mutations Detects 97% of Cystic Fibrosis (CF) Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Mutation Rare diseases Tay–Sachs disease Cystic fibrosis ΔF508 Point mutation Ashkenazi Jews Nonsense mutation Medical genetics of Jewish people Biology Health Genetics
32	Cystic Fibrosis: Pathogenesis and Future Treatment Strategies Felix A Ratjen MD PhD FRCP(C) Add to Reading List Source URL: www.rcjournal.com Language: English - Date: 2009-04-24 03:41:10 Pancreas disorders Channelopathy Cystic fibrosis Pediatrics Denufosol Epithelial sodium channel ΔF508 Mucociliary clearance Chloride channel Biology Health Anatomy
33	Brazilian Journal of Medical and Biological Research[removed]: 11-15 Cystic fibrosis mutations in the North of Brazil ISSN 0100-879X Add to Reading List Source URL: www.scielo.br Language: English - Date: 2006-02-13 14:28:35 Mutation Pancreas disorders Pediatrics Rare diseases Cystic fibrosis ΔF508 Nonsense mutation Genetic testing Ivacaftor Health Genetics Biology
34	PDF Document Add to Reading List Source URL: physrev.physiology.org Language: English Signal transduction Cystic fibrosis transmembrane conductance regulator Protein kinase C Cystic fibrosis Phosphorylation ΔF508 Protein kinase A Ion channel ATP-binding cassette transporter Biology Protein kinases ABC transporters