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White matter abnormalities in the Hdc knockout mouse, a model of tic and OCD pathophysiology
INTRODUCTION: An inactivating mutation in the histidine decarboxylase gene (Hdc) has been identified as a rare but high-penetrance genetic cause of Tourette syndrome (TS). TS is a neurodevelopmental syndrome characterized by recurrent motor and vocal tics; it is accompanied by structural and functio...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731796/ https://www.ncbi.nlm.nih.gov/pubmed/36504678 http://dx.doi.org/10.3389/fnmol.2022.1037481 |