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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...
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| Publicado no: | J Neurodev Disord |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6683428/ https://ncbi.nlm.nih.gov/pubmed/31387522 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-019-9278-9 |
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