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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292032/ https://www.ncbi.nlm.nih.gov/pubmed/25518740 http://dx.doi.org/10.1038/jhg.2014.107 |