Distribution patterns of the delta F508 mutation in the CFTR gene of CF-linked marker haplotypes in the German population.

Journal: Human Genetics
Published:
Abstract

We have measured the frequency of the delta F508 mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and its association with cystic fibrosis (CF)-linked marker haplotypes in the German population. Based on the analysis of 400 CF chromosomes, the frequency of the delta F508 mutation is estimated to be 77.3%, the vast majority being associated with marker haplotype KM19-XV2c 2 1. Our data further suggest the presence of another frequent CF mutation associated with this marker haplotype.

Authors
A Reis, S Bremer, M Schlösser, M Dueck, I Böhm, J Hundrieser, M Macek, M Stuhrmann, M Wagner, T Dörk
Relevant Conditions

Cystic Fibrosis