Frequency of delta-F508 mutation and XV2C/KM19 haplotypes in Cuban cystic fibrosis families.

Journal: Human Heredity
Published:
Abstract

We tested the frequency of the delta F508 mutation and haplotypes linked to the cystic fibrosis (CF) gene in Cuba. The delta F508 deletion was detected in 34.0% of the CF chromosomes. There was a shortage of delta F508 heterozygotes, suggesting non-randomness in mating patterns. Haplotype B (XV2C/KM19 1/2) was found on 40.5% of the CF chromosomes (71.5% of delta F508 chromosomes, 28.3% of non-delta F508 CF chromosomes) against 13.5% of non-CF chromosomes.

Authors
T Collazo, C Magarino, R Chavez, B Suardiaz, S Gispert, M Gomez, M Rojo, L Heredero
Relevant Conditions

Cystic Fibrosis