TRANSFORMATIVE THERAPIES FOR RARE CFTR MISSENSE ALLELES

Những quyển sách tương tự

• Functional studies of rare missense mutations in CFTR facilitate interpretation of genotype-phenotype relationships
  Bằng: Krasnov, Kristina V., et al.
  Được phát hành: (2008)
• Missense variants in CFTR nucleotide-binding domains predict quantitative phenotypes associated with cystic fibrosis disease severity
  Bằng: Masica, David L., et al.
  Được phát hành: (2015)
• Assessing the Disease-Liability of Mutations in CFTR
  Bằng: Ferec, Claude, et al.
  Được phát hành: (2012)
• Residual function of cystic fibrosis mutants predicts response to small molecule CFTR modulators
  Bằng: Han, Sangwoo T., et al.
  Được phát hành: (2018)
• Most Rare Missense Alleles Are Deleterious in Humans: Implications for Complex Disease and Association Studies
  Bằng: Kryukov, Gregory V., et al.
  Được phát hành: (2007)