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7. Twenty years after cystic fibrosis gene identification: Where are we and what are we up to? Edelman A; Fritsch J; Ollero M Pathol Biol (Paris); 2011 Jun; 59(3):131-3. PubMed ID: 19896304 [No Abstract] [Full Text] [Related]
8. Insights into the mechanisms underlying CFTR channel activity, the molecular basis for cystic fibrosis and strategies for therapy. Kim Chiaw P; Eckford PD; Bear CE Essays Biochem; 2011 Sep; 50(1):233-48. PubMed ID: 21967060 [TBL] [Abstract][Full Text] [Related]
9. A new frameshift mutation 460delG in exon 4 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Wagner K; Schneditz P; Rosenkranz W Hum Mutat; 1996; 7(2):183. PubMed ID: 8829644 [No Abstract] [Full Text] [Related]
10. [CFTR protein and molecular mechanisms of pulmonary involvement in cystic fibrosis]. Chinet T Rev Pneumol Clin; 1995; 51(3):122-9. PubMed ID: 7569573 [TBL] [Abstract][Full Text] [Related]
11. Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this cystic fibrosis transmembrane conductance regulator mutation does not cause cystic fibrosis. Derichs N; Schuster A; Grund I; Ernsting A; Stolpe C; Körtge-Jung S; Gallati S; Stuhrmann M; Kozlowski P; Ballmann M Clin Genet; 2005 Jun; 67(6):529-31. PubMed ID: 15857421 [No Abstract] [Full Text] [Related]
12. Pharmacologic approaches to correcting the basic defect in cystic fibrosis. Lukacs GL; Durie PR N Engl J Med; 2003 Oct; 349(15):1401-4. PubMed ID: 14534332 [No Abstract] [Full Text] [Related]
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14. A novel nonsense mutation, S466Xa in exon 10 of the cystic fibrosis transmembrane conductance regulator gene. Mittre H; Barre M; Leymarie P Hum Mutat; 1996; 8(4):392-3. PubMed ID: 8956053 [No Abstract] [Full Text] [Related]
15. [Cystic fibrosis: the CFTR gene, its mutations, the genetic counseling]. Goossens M; Ghanem N; Girodon E; Costes B; Fanen P Rev Pneumol Clin; 1995; 51(3):130-6. PubMed ID: 7569574 [TBL] [Abstract][Full Text] [Related]