Sign Up to like & get
recommendations!
2
Published in 2019 at "Molecular Autism"
DOI: 10.1186/s13229-019-0303-3
Abstract: BackgroundAutism 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,…
read more here.
Keywords:
neurons derived;
ca2 transients;
increased ca2;
derived asd ... See more keywords