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Vol. 44, No. 3, 1994
Issue release date: 1994
Hum Hered 1994;44:169–171
Short Communication

Low Frequency of the ΔF508 Mutation in Finno-Ugrian and Baltic Populations

Wennberg C.a · Kucinskas V.b
aDepartment of Medical Genetics, University of Umeå, Sweden; and bCenter of Human Genetics, Vilnius University, Lithuania


The frequency of carriers of the ΔF508 mutation at the cystic fibrosis (CF) locus was studied in population samples of Finns, Lithuanians, Saamis (Lapps) and Swedes from northern Sweden. The carrier frequencies in northern Sweden (1:200) and in Lithuanians (1:143) were significantly lower than in southern Scandinavia (Denmark; 1:38). No ΔF508 carriers were found in Finns (n = 171) and Saamis (n = 151). The results indicate that the frequency of ΔF508 is low in Finno-Ugrian and Baltic populations, and the decreased frequency of ΔF508 in northern Sweden may be due to Finnish and Saamish admixture.

 goto top of outline Author Contacts

C. Wennberg, MD, Department of Medical Genetics, University of Umeå, S-90185 Umeå (Sweden)

 goto top of outline Article Information

Received: October 11, 1993
Revised: October 29, 1993
Accepted: November 2, 1993
Published online: September 03, 2008
Number of Print Pages : 3

 goto top of outline Publication Details

Human Heredity (International Journal of Human and Medical Genetics)

Vol. 44, No. 3, Year 1994 (Cover Date: 1994)

Journal Editor: Devoto M. (Philadelphia, Pa.)
ISSN: 0001–5652 (Print), eISSN: 1423–0062 (Online)

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