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Article

PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure.

Journal of human genetics - 1 Mar 2015

Belyk Michel, Kraft Shelly Jo, Brown Steven

Abstract excerpt

PlexinA is a neuronal receptor protein that facilitates axon guidance during embryogenesis. This gene is associated with several neurological disorders including Alzheimer's disease, Parkinson's disease and autism. However, the effect of variants of PlexinA on brain structure remains unclear. We...

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Identifiers

PMID: 25518740
DOI: 10.1038/jhg.2014.107
PMCID: PMC5292032

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25518740-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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