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Neurodevelopmental Profile of Siblings with Angelman Syndrome due to pathogenic UBE3A variants
BACKGROUND: Angelman syndrome (AS) is a neurodevelopmental disorder caused by a lack of expression of the maternally-inherited UBE3A gene on chromosome 15. Individuals with AS due to a UBE3A mutation are more likely to have siblings who also have AS compared to those with AS due to other cytogenetic...
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| Izdano u: | J Intellect Disabil Res |
|---|---|
| Glavni autori: | , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2019
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8020893/ https://ncbi.nlm.nih.gov/pubmed/31854050 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jir.12700 |
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