Pathway-specific dopaminergic deficits in a mouse model of Angelman syndrome

Angelman syndrome (AS) is a neurodevelopmental disorder caused by maternal deletions or mutations of the ubiquitin ligase E3A (UBE3A) allele and characterized by minimal verbal communication, seizures, and disorders of voluntary movement. Previous studies have suggested that abnormal dopamine neurot...

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Bibliografische gegevens
Hoofdauteurs: Riday, Thorfinn T., Dankoski, Elyse C., Krouse, Michael C., Fish, Eric W., Walsh, Paul L., Han, Ji Eun, Hodge, Clyde W., Wightman, R. Mark, Philpot, Benjamin D., Malanga, C.J.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Clinical Investigation 2012
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Research Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3533533/
https://ncbi.nlm.nih.gov/pubmed/23143301
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI61888
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