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The Mental Retardation Protein PAK3 Contributes to Synapse Formation and Plasticity in Hippocampus
Mutations of the gene coding for PAK3 (p21-activated kinase 3) are associated with X-linked, nonsyndromic forms of mental retardation (MRX) in which the only distinctive clinical feature is the cognitive deficit. The mechanisms through which PAK3 mutation produces the mental handicap remain unclear,...
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| Publié dans: | J Neurosci |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Society for Neuroscience
2004
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6730202/ https://ncbi.nlm.nih.gov/pubmed/15574732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.2931-04.2004 |
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