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Article

Huntington disease in Finland: a molecular and genealogical study.

Human genetics - 1 May 1992

Ikonen E, Ignatius J, Norio R, Palo J, Peltonen L

Abstract excerpt

Huntington disease (HD) is found at exceptionally low frequency in the Finnish population. In this population, linkage disequilibrium was earlier established with markers from the D4S10 and D4S43 loci. We now report a continuation to the restriction fragment length polymorphism haplotype analysis, in combination with a genealogical study of all the Finnish HD families. When the HD pedigrees were systematically...

Topics

Chromosomes, Human, Pair 4
Female
Finland
Genetic Markers
Haplotypes
Humans
Huntington Disease
Male
Mutation
Pedigree
Polymorphism, Restriction Fragment Length
Risk

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 1351031
DOI: 10.1007/BF00220539

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-1351031-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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