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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...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2021
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| 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 |