Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis gene.

Documenti analoghi

• Genetic determination of exocrine pancreatic function in cystic fibrosis.
  di: Kristidis, P, et al.
  Pubblicazione: (1992)
• Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator.
  di: Smit, L S, et al.
  Pubblicazione: (1993)
• A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
  di: Zielenski, J, et al.
  Pubblicazione: (1991)
• Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X
  di: Aznarez, Isabel, et al.
  Pubblicazione: (2007)
• A mutation in the second nucleotide binding fold of the cystic fibrosis gene.
  di: Osborne, L, et al.
  Pubblicazione: (1991)