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An autism-linked missense mutation in SHANK3 reveals the modularity of Shank3 function
Genome sequencing has revealed an increasing number of genetic variations that are associated with neuropsychiatric disorders. Frequently, studies limit their focus to likely gene-disrupting mutations because they are relatively easy to interpret. Missense variants, instead, have often been underval...
Shranjeno v:
| izdano v: | Mol Psychiatry |
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| Main Authors: | , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6609509/ https://ncbi.nlm.nih.gov/pubmed/30610205 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41380-018-0324-x |
| Oznake: |
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