Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders

Shared developmental gait disruptions across two mouse models of neurodevelopmental disorders

Abstract 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...

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Bibliographic Details
Main Authors: Rachel M. Rahn, Claire T. Weichselbaum, David H. Gutmann, Joseph D. Dougherty, Susan E. Maloney
Format: Article
Language:English
Published: BMC 2021-03-01
Series:Journal of Neurodevelopmental Disorders
Subjects:
Gait
Williams Syndrome
Neurofibromatosis Type 1
mice
precision medicine
neurodevelopmental disorders
Online Access:https://doi.org/10.1186/s11689-021-09359-0

Internet

https://doi.org/10.1186/s11689-021-09359-0

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