Skip to main content
Log in

The mutation ΔF508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis

  • Population analysis of the major mutation in cystic fibrosis
  • Published:
Human Genetics Aims and scope Submit manuscript

Summary

We tested 190 chromosomes from Dutch cystic fibrosis (CF) patients and carriers for the presence or absence of the major CF mutation ΔF508. This mutation was found on 77% of the Dutch CF chromosomes. We observed a significant difference in the distribution of the ages at diagnosis between homozygotes for ΔF508 and the other patients. ΔF508 homozygotes tend to be identified as patients at neonatal or infantile age. The age at diagnosis of patients with at least one unknown allele, on the other hand, ranged between neonatal and young adult age.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Halley, D.J.J., Veeze, H.J., Sandkuyl, L.A. et al. The mutation ΔF508 on Dutch cystic fibrosis chromosomes: frequency and relation to patients age at diagnosis. Hum Genet 85, 407–408 (1990). https://doi.org/10.1007/BF02428281

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02428281

Keywords

Navigation