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Article

Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.

European journal of human genetics : EJHG - 1 Apr 2002

He Bing, Giedraitis Vilmantas, Ligers Arturs, Binzer Michael, Andersen Peter M, Forsgren Lars, Sandkuijl Lodewijk A, Hillert Jan

Abstract excerpt

Multiple sclerosis (MS) is a chronic inflammatory disease resulting in demyelination in the central nervous system (CNS). Increasing evidence supports that genetic factors confer susceptibility to MS. One locus, the HLA complex (6p21), has been identified as important in MS, but no other loci hav...

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Share to Chromosomes, Human, Pair 17
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 12032736
DOI: 10.1038/sj.ejhg.5200802

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12032736-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.PMID 12032736Read ↗

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