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PMID: 1976595 Published · ppublish English Journal Article

The frequency of the delta F508 mutation on cystic fibrosis chromosomes in Israeli families: correlation to CF haplotypes in Jewish communities and Arabs.

Human genetics ·Vol. 85 ·No. 4 ·1990-09-00 ·Pages 416-7

Lerer I, Cohen S, Chemke M, Sanilevich A, Rivlin J, Golan A, Yahav J, Friedman A, Abeliovich D

Abstract

We have analysed the distribution of the delta F508 mutation and the haplotypes of cystic fibrosis (CF) bearing chromosomes among the Israeli CF population. The population was classified according to its ethnic origin and included 3 groups, Ashkenazi Jews, Sephardic/Oriental Jews and Arabs. Haplotype B (KM19 allele 2, XV2c allele 1) was found to be the predominant haplotype in all groups but in each of them the haplotype distribution was different. The delta F508 mutation was present in all groups and accounts for 32% of the CF mutations. It was mainly associated with the B haplotype but only one third of the CF chromosomes with this haplotype carry the delta F508 mutation.

MeSH Terms
Chromosome Deletion Cystic Fibrosis/epidemiology,genetics Ethnicity Gene Frequency Humans Israel/epidemiology Jews Polymorphism, Restriction Fragment Length
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Lerer I
Department of Human Genetics, Hadassah University Hospital, Jerusalem, Israel.
Cohen S
Chemke M
Sanilevich A
Rivlin J
Golan A
Yahav J
Friedman A
Abeliovich D
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1990-09-00
Pages
416-7
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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