High frequency of cystic fibrosis transmembrane regulator mutation L997F in patients with recurrent idiopathic pancreatitis and in newborns with hypertrypsinemia.

Samankaltaisia teoksia

• Cystic fibrosis mutations in heterozygous newborns with hypertrypsinemia and low sweat chloride.
  Tekijä: Castellani, C, et al.
  Julkaistu: (1999)
• Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in neonatal hypertrypsinaemia with normal sweat test
  Tekijä: CASTELLANI, C., et al.
  Julkaistu: (2001)
• Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis
  Tekijä: Castellani, C, et al.
  Julkaistu: (2000)
• CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test.
  Tekijä: Castellani, C, et al.
  Julkaistu: (1997)
• An unstable transmembrane segment in the cystic fibrosis transmembrane conductance regulator.
  Tekijä: Tector, M, et al.
  Julkaistu: (1999)