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PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure

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 uncle...

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Bibliographische Detailangaben
Veröffentlicht in:J Hum Genet
Hauptverfasser: Belyk, Michel, Kraft, Shelly Jo, Brown, Steven
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2014
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5292032/
https://ncbi.nlm.nih.gov/pubmed/25518740
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/jhg.2014.107
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