Major motor and gait deficits with sexual dimorphism in a Shank3 mutant mouse model
Abstract Background Contrasting findings were reported in several animal models with a Shank3 mutation used to induce various autism spectrum disorder (ASD) symptoms. Here, we aimed at investigating behavioral, cellular, and molecular consequences of a C-terminal (frameshift in exon 21) deletion in...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2021-01-01
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Series: | Molecular Autism |
Subjects: | |
Online Access: | https://doi.org/10.1186/s13229-020-00412-8 |