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STXBP1-associated neurodevelopmental disorder: a comparative study of behavioural characteristics
Abstract 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 s...
שמור ב:
| Main Authors: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BMC
2019-08-01
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| סדרה: | Journal of Neurodevelopmental Disorders |
| נושאים: | |
| גישה מקוונת: | http://link.springer.com/article/10.1186/s11689-019-9278-9 |
| תגים: |
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