Neural Markers of Auditory Response and Habituation in Phelan-McDermid Syndrome

Phelan-McDermid Syndrome (PMS) is a rare genetic disorder caused by deletion or sequence variation in the SHANK3 gene at terminal chromosome 22 that confers high likelihood of comorbid autism spectrum disorder (ASD). Whereas individuals with idiopathic ASD (iASD) can demonstrate diverse patterns of...

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Detalles Bibliográficos
Autores principales: Isenstein, Emily L., Grosman, Hannah E., Guillory, Sylvia B., Zhang, Yian, Barkley, Sarah, McLaughlin, Christopher S., Levy, Tess, Halpern, Danielle, Siper, Paige M., Buxbaum, Joseph D., Kolevzon, Alexander, Foss-Feig, Jennifer H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110667/
https://www.ncbi.nlm.nih.gov/pubmed/35592263
http://dx.doi.org/10.3389/fnins.2022.815933

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110667/
https://www.ncbi.nlm.nih.gov/pubmed/35592263
http://dx.doi.org/10.3389/fnins.2022.815933

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