Neural selectivity for communicative auditory signals in Phelan-McDermid syndrome

BACKGROUND: Phelan-McDermid syndrome (PMS), a neurodevelopmental disorder caused by deletion or mutation in the SHANK3 gene, is one of the more common single-locus causes of autism spectrum disorder (ASD). PMS is characterized by global developmental delay, hypotonia, delayed or absent speech, incre...

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Detalles Bibliográficos
Publicado en:J Neurodev Disord
Autores principales: Wang, A. Ting, Lim, Teresa, Jamison, Jesslyn, Bush, Lauren, Soorya, Latha V., Tavassoli, Teresa, Siper, Paige M., Buxbaum, Joseph D., Kolevzon, Alexander
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2016
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Research
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4763436/
https://ncbi.nlm.nih.gov/pubmed/26909118
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-016-9138-9
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