HAL (France)open access
Autism Spectrum Disorder phenotype and underlying pathological mechanisms in mice modeling human mutations of the SCN2A gene
Autism Spectrum Disorder, Sodium channels, Scn2a, Excitabilité neuronale, Canaux sodiques, 0, 2, Modèles murins
This document is indexed with metadata only — full text is not available in the archive for this record.
Open the official source ↗
Record · ID 1120661
Retrieved via
Conceptio — every document is proof-bundled with source, license, and retrieval metadata.