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STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
BACKGROUND: De novo loss of function mutations in STXBP1 are a relatively common cause of epilepsy and intellectual disability (ID). However, little is known about the types and severities of behavioural features associated with this genetic diagnosis. METHODS: To address this, we collected systemat...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6683428/ https://www.ncbi.nlm.nih.gov/pubmed/31387522 http://dx.doi.org/10.1186/s11689-019-9278-9 |