SHANK3 Genotype Mediates Speech and Language Phenotypes in a Nonclinical Population

Mutations affecting the synaptic-scaffold gene SHANK3 represent the most common genetic causes of autism with intellectual disability, accounting for about 1-2% of cases. Rare variants of this gene have also been associated with schizophrenia, and its deletion results in the autistic condition known...

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Detalles Bibliográficos
Autores principales: Manning, Christina, Hurd, Peter L., Read, Silven, Crespi, Bernard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195663/
https://www.ncbi.nlm.nih.gov/pubmed/34188957
http://dx.doi.org/10.1155/2021/6634584

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195663/
https://www.ncbi.nlm.nih.gov/pubmed/34188957
http://dx.doi.org/10.1155/2021/6634584

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