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Paper Details

Thorase variants are associated with defects in glutamatergic neurotransmission that can be rescued by Perampanel.
Sci Transl Med
16
2017
-, 5, 5-methyl-4-isoxazolepropionic acid, 5-methyl-4-isoxazolepropionic acid receptors, AAA+, AMPAR, AMPAR subunit, AMPARs, ATAD1, ATPase, GluA2, Perampanel, Thorase, Thorase variants, Thorase-deficient, adenosine, adenosine triphosphatase, amino-3-hydroxy-, exons, mice, mouse, mouse primary cortical neurons, patients, schizophrenia
Author NameAffiliation
Dimitrios AvramopoulosJohns Hopkins University School of Medicine
Dimitrios AvramopoulosMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
David ValleMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine
David ValleJohns Hopkins University School of Medicine
Ted M DawsonInstitute for Cell Engineering, Johns Hopkins University School of Medicine
Ted M DawsonJohns Hopkins University School of Medicine
Ted M DawsonJohns Hopkins University School of Medicine
Ted M DawsonJohns Hopkins University School of Medicine
Ted M DawsonInstitute for Cell Engineering, Johns Hopkins University School of Medicine
Ted M DawsonJohns Hopkins University School of Medicine
Ted M DawsonJohns Hopkins University School of Medicine
Ted M DawsonJohns Hopkins University School of Medicine
Valina L DawsonInstitute for Cell Engineering, Johns Hopkins University School of Medicine
Valina L DawsonJohns Hopkins University School of Medicine
Valina L DawsonJohns Hopkins University School of Medicine
Valina L DawsonJohns Hopkins University School of Medicine
Valina L DawsonInstitute for Cell Engineering, Johns Hopkins University School of Medicine
Valina L DawsonJohns Hopkins University School of Medicine
Valina L DawsonJohns Hopkins University School of Medicine
Valina L DawsonJohns Hopkins University School of Medicine
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