First report of three cystic fibrosis patients homozygous for the 1717-1G-->A mutation.

مواد مشابهة

• A cystic fibrosis patient with the nonsense mutation G542X and the splice site mutation 1717-1.
  بواسطة: Schloesser, M, وآخرون
  منشور في: (1991)
• Genotype-phenotype correlation in five cystic fibrosis patients homozygous for the 621 + 1G-->T mutation.
  بواسطة: De Braekeleer, M, وآخرون
  منشور في: (1997)
• Heterogeneity of phenotype in two cystic fibrosis patients homozygous for the CFTR exon 11 mutation G551D.
  بواسطة: Parad, R B
  منشور في: (1996)
• Severe cystic fibrosis in a child homozygous for the G542 nonsense mutation in the CFTR gene.
  بواسطة: Bienvenu, T, وآخرون
  منشور في: (1993)
• Homozygous nonsense mutation causing cystic fibrosis with uniparental disomy.
  بواسطة: Beaudet, A L, وآخرون
  منشور في: (1991)