Mechanisms underlying the EEG biomarker in Dup15q syndrome

BACKGROUND: Duplications of 15q11.2-q13.1 (Dup15q syndrome), including the paternally imprinted gene UBE3A and three nonimprinted gamma-aminobutyric acid type-A (GABA(A)) receptor genes, are highly penetrant for neurodevelopmental disorders such as autism spectrum disorder (ASD). To guide targeted t...

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書目詳細資料
發表在:Mol Autism
Main Authors: Frohlich, Joel, Reiter, Lawrence T., Saravanapandian, Vidya, DiStefano, Charlotte, Huberty, Scott, Hyde, Carly, Chamberlain, Stormy, Bearden, Carrie E., Golshani, Peyman, Irimia, Andrei, Olsen, Richard W., Hipp, Joerg F., Jeste, Shafali S.
格式: Artigo
語言:Inglês
出版: BioMed Central 2019
主題:
Research
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6609401/
https://ncbi.nlm.nih.gov/pubmed/31312421
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-019-0280-6
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