Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders

BACKGROUND: Motor deficits such as abnormal gait are an underappreciated yet characteristic phenotype of many neurodevelopmental disorders (NDDs), including Williams Syndrome (WS) and Neurofibromatosis Type 1 (NF1). Compared to cognitive phenotypes, gait phenotypes are readily and comparably assesse...

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Detalles Bibliográficos
Autores principales: Rahn, Rachel M., Weichselbaum, Claire T., Gutmann, David H., Dougherty, Joseph D., Maloney, Susan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980331/
https://www.ncbi.nlm.nih.gov/pubmed/33743598
http://dx.doi.org/10.1186/s11689-021-09359-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980331/
https://www.ncbi.nlm.nih.gov/pubmed/33743598
http://dx.doi.org/10.1186/s11689-021-09359-0

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