Electrophysiological phenotype in Angelman syndrome differs between genotypes

BACKGROUND: Angelman syndrome is a severe neurodevelopmental disorder caused by either disruptions of the gene UBE3A or deletion of chromosome 15 at 15q11-q13, which encompasses UBE3A and several other genes, including GABRB3, GABRA5, GABRG3 encoding GABA type-A receptor (GABA(A)R) subunits (β3, α5,...

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Detalhes bibliográficos
Publicado no:Biol Psychiatry
Main Authors: Frohlich, Joel, Miller, Meghan, Bird, Lynne M., Garces, Pilar, Purtell, Hannah, Hoener, Marius C., Philpot, Benjamin D., Sidorov, Michael S., Tan, Wen-Hann, Hernandez, Maria-Clemencia, Rotenberg, Alexander, Jeste, Shafali S., Krishnan, Michelle, Khwaja, Omar, Hipp, Joerg F.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6482952/
https://ncbi.nlm.nih.gov/pubmed/30826071
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2019.01.008
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