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Cockayne syndrome-derived neurons display reduced synapse density and altered neural network synchrony
Cockayne syndrome (CS) is a rare genetic disorder in which 80% of cases are caused by mutations in the Excision Repair Cross-Complementation group 6 gene (ERCC6). The encoded ERCC6 protein is more commonly referred to as Cockayne Syndrome B protein (CSB). Classical symptoms of CS patients include fa...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4787902/ https://ncbi.nlm.nih.gov/pubmed/26755826 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw008 |
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