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Behavior and neuropsychiatric manifestations in Angelman syndrome

Angelman syndrome has been suggested as a disease model of neurogenetic developmental condition with a specific behavioral phenotype. It is due to lack of expression of the UBE3A gene, an imprinted gene located on chromosome 15q. Here we review the main features of this phenotype, characterized by h...

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Bibliografski detalji
Glavni autori: Pelc, Karine, Cheron, Guy, Dan, Bernard
Format: Artigo
Jezik:Inglês
Izdano: Dove Medical Press 2008
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2526368/
https://ncbi.nlm.nih.gov/pubmed/18830393
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