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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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Publicado no: | J Neurodev Disord |
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Principais autores: | , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
BioMed Central
2016
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Assuntos: | |
Acesso em linha: | 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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