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Article

IGHV4-39 deletion polymorphism does not associate with risk or outcome of multiple sclerosis.

Journal of neuroimmunology - 25 Aug 2010

Watson Corey T, Ramagopalan Sreeram V, Morrison Katie M, Ebers George C, Breden Felix

Abstract excerpt

The restricted use of immunoglobulin heavy chain variable (IGHV) family 4 gene segments by clonally expanded B cells in brain lesions and cerebrospinal fluid (CSF) of multiple sclerosis (MS) patients is well documented. Specifically, the overrepresentation of gene IGHV4-39 has been highlighted in...

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Share to Genetic Predisposition to Disease
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20471699
DOI: 10.1016/j.jneuroim.2010.04.012

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20471699-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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