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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609401/
https://www.ncbi.nlm.nih.gov/pubmed/31312421
http://dx.doi.org/10.1186/s13229-019-0280-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609401/
https://www.ncbi.nlm.nih.gov/pubmed/31312421
http://dx.doi.org/10.1186/s13229-019-0280-6

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