A carregar...
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...
Na minha lista:
| Publicado no: | J Intellect Disabil Res |
|---|---|
| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
|
| Assuntos: | |
| Acesso em linha: | 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 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|