Human Neuropsychiatric Disease Modeling using Conditional Deletion Reveals Synaptic Transmission Defects Caused by Heterozygous Mutations in NRXN1.
Cell stem cell | 2015-09-03 | PMID 26279266
Pak ChangHui, Danko Tamas, Zhang Yingsha and 6 more
Genes: NRXN1, CASK
