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Paper Details

SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
Nat Commun
5
2022
SLITRK2, SLITRK2 variants, SLITRK2 wild-type, Slitrk2, TrkB, X chromosome, X-linked neurodevelopmental disorders, abnormal gait, mice, neurodevelopmental disorders, neurons, patients, postsynaptic neurons, receptor tyrosine kinase, tyrosine
Author NameAffiliation
Julia WynnColumbia University Medical Center
Wendy K ChungColumbia University Medical Center
Wendy K ChungColumbia University
Wendy K ChungColumbia University Medical Center
Wendy K ChungColumbia University
Angelo SelicorniCenter for Fragile Child, ASST Lariana Sant'Anna Hospital
Jean MullerInstitut de Genetique Medicale d'Alsace (IGMA), Universite de Strasbourg et INSERM
Jean MullerInstitut de Genetique Medicale d'Alsace (IGMA), Hopitaux Universitaires de Strasbourg
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