Association of less common cystic fibrosis mutations with a mild phenotype.

Documenti analoghi

• Mild cystic fibrosis phenotype in patients with the 3272-26A > G mutation.
  di: Kanavakis, E, et al.
  Pubblicazione: (1995)
• Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%.
  di: Macek, M, et al.
  Pubblicazione: (1997)
• Cystic fibrosis. 3. Cloning the cystic fibrosis gene: implications for diagnosis and treatment.
  di: Porteous, D. J., et al.
  Pubblicazione: (1991)
• Cystic fibrosis mutations and disease phenotype
  di: TAYLOR, C, et al.
  Pubblicazione: (2000)
• Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani family.
  di: Curtis, A, et al.
  Pubblicazione: (1993)