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A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability
The large majority of cases with intellectual disability are syndromic (i.e. occur with other well-defined clinical phenotypes) and have been studied extensively. Autosomal recessive nonsyndromic intellectual disability is a group of genetically heterogeneous disorders for which a number of potentia...
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| Wydane w: | Front Psychiatry |
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| Główni autorzy: | , , , , , , , |
| Format: | Artigo |
| Język: | Inglês |
| Wydane: |
Frontiers Media S.A.
2020
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| Hasła przedmiotowe: | |
| Dostęp online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7247441/ https://ncbi.nlm.nih.gov/pubmed/32499722 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fpsyt.2020.00354 |
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