Genetically encoded impairment of neuronal KCC 2 cotransporter function in human idiopathic generalized epilepsy

Author:

Kahle Kristopher T12,Merner Nancy D34,Friedel Perrine56,Silayeva Liliya7,Liang Bo8,Khanna Arjun2,Shang Yuze12,Lachance‐Touchette Pamela9,Bourassa Cynthia9,Levert Annie4,Dion Patrick A310,Walcott Brian2,Spiegelman Dan4,Dionne‐Laporte Alexandre4,Hodgkinson Alan11,Awadalla Philip1112,Nikbakht Hamid13,Majewski Jacek13,Cossette Patrick9,Deeb Tarek Z7,Moss Stephen J7,Medina Igor56,Rouleau Guy A4

Affiliation:

1. Department of Cardiology Manton Center for Orphan Disease Research Howard Hughes Medical Institute Boston Children's Hospital Boston MA USA

2. Department of Neurosurgery Massachusetts General Hospital Boston MA USA

3. Department of Drug Discovery and Development Harrison School of Pharmacy Auburn University Auburn AL USA

4. Department of Neurology and Neurosurgery Montreal Neurological Hospital and Institute McGill Université Montréal QC Canada

5. INMED INSERM Unité 901 Marseille France

6. Aix‐Marseille Université UMR 901 Marseille France

7. Department of Neuroscience Tufts University School of Medicine Boston MA USA

8. Department of Biological Chemistry and Molecular Pharmacology (BCMP) Harvard Medical School Boston MA USA

9. Center of Research of the Université de Montréal and the Department of Medicine Université de Montréal Montréal QC Canada

10. Department of Pathology and Cell Biology Université de Montréal Montréal QC Canada

11. CHU Sainte Justine Research Centre Department of Pediatrics Faculty of Medicine Université de Montréal Montréal QC Canada

12. CARTaGENE Montréal QC Canada

13. Department of Human Genetics McGill University and Genome Quebec Innovation Centre Montréal QC Canada

Publisher

EMBO

Subject

Genetics,Molecular Biology,Biochemistry

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