Increased Ca2+ signaling in NRXN1α +/− neurons derived from ASD induced pluripotent stem cells
Abstract Background Autism spectrum disorder (ASD) is a neurodevelopmental disorder with a high co-morbidity of epilepsy and associated with hundreds of rare risk factors. NRXN1 deletion is among the commonest rare genetic factors shared by ASD, schizophrenia, intellectual disability, epilepsy, and...
Main Authors: | , , , , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2019-12-01
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Series: | Molecular Autism |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13229-019-0303-3 |