Mitochondrial dysfunction and oxidative stress contribute to cognitive and motor impairment in FOXP1 syndrome
Work
Year: 2022
Type: article
Abstract: FOXP1 syndrome caused by haploinsufficiency of the forkhead box protein P1 (FOXP1) gene is a neurodevelopmental disorder that manifests motor dysfunction, intellectual disability, autism, and language... more
Authors Jing Wang, Henning Fröhlich, Felipe Bodaleo Torres, Rangel L. Silva, Gernot Poschet +2 more
Institutions Heidelberg University, University Hospital Heidelberg, Chica and Heinz Schaller Foundation
Cites: 79
Cited by: 44
Related to: 10
FWCI: 5.789
Citation percentile (by year/subfield): 99.98
Subfield: Neurology
Field: Neuroscience
Domain: Life Sciences
Sustainable Development Goal Affordable and clean energy
Open Access status: hybrid
Funder China Scholarship Council
Grant ID #201708230108