CFTR mutation analysis and haplotype associations in CF patients()

مواد مشابهة

• Newborn Screening Quality Assurance Program for CFTR Mutation Detection and Gene Sequencing to Identify Cystic Fibrosis
  بواسطة: Hendrix, Miyono M., وآخرون
  منشور في: (2016)
• Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patients.
  بواسطة: Verlingue, C, وآخرون
  منشور في: (1998)
• Complementation of null CF mice with a human CFTR YAC transgene.
  بواسطة: Manson, A L, وآخرون
  منشور في: (1997)
• Therapeutic benefit observed with the CFTR potentiator, ivacaftor, in a CF patient homozygous for the W1282X CFTR nonsense mutation
  بواسطة: Mutyam, Venkateshwar, وآخرون
  منشور في: (2016)
• Phenotypes of California CF Newborn Screen-Positive Children with CFTR 5T Allele by TG Repeat Length
  بواسطة: Salinas, Danieli Barino, وآخرون
  منشور في: (2016)