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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...
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| 出版年: | Autism Res Treat |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Hindawi
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8195663/ https://ncbi.nlm.nih.gov/pubmed/34188957 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2021/6634584 |
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