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Disease Models & Mechanisms
(Sep 2023)
AGAP1-associated endolysosomal trafficking abnormalities link gene–environment interactions in neurodevelopmental disorders
Sara A. Lewis,
Somayeh Bakhtiari,
Jacob Forstrom,
Allan Bayat,
Frédéric Bilan,
Gwenaël Le Guyader,
Ebba Alkhunaizi,
Hilary Vernon,
Sergio R. Padilla-Lopez,
Michael C. Kruer
Affiliations
Sara A. Lewis
Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA
Somayeh Bakhtiari
Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA
Jacob Forstrom
Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA
Allan Bayat
Institute for Regional Health Services, University of Southern Denmark, 5230 Odense, Denmark
Frédéric Bilan
Service de Génétique, CHU de Poitiers, 86000 Poitiers, France
Gwenaël Le Guyader
Service de Génétique, CHU de Poitiers, 86000 Poitiers, France
Ebba Alkhunaizi
Department of Medical Genetics, North York General Hospital, Toronto, ON M3J0K2, Canada
Hilary Vernon
Department of Genetic Medicine, Johns Hopkins University, Baltimore, MD, USA
Sergio R. Padilla-Lopez
Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA
Michael C. Kruer
Pediatric Movement Disorders Program, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ 85016, USA
DOI
https://doi.org/10.1242/dmm.049838
Journal volume & issue
Vol. 16, no. 9
Abstract
Read online
No abstracts available.
Keywords
drosophila
agap1
synaptic morphology
endolysosome
autophagy
eif2α
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