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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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Mol Autism |
|---|---|
| Prif Awduron: | , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2019
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| Pynciau: | |
| Mynediad Ar-lein: | 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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