Skip to Main Content

Paper Details

Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis.
Neurol Genet
38
2015
COS-7 cells, DNM1, Dnm1, Dnm1 (, Epileptic encephalopathy, Ftfl, G, G-, G359A, GTPase, HeLa, epilepsies, epileptic encephalopathy, mice, mouse, mutant DNM1, mutant DNM1-transfected HeLa cells, neuronal, transferrin, wild-type and mutant DNM1 constructs
Author NameAffiliation
Erin L HeinzenDuke University School of Medicine (R.S.D., NC Institute for Genomic Medicine (E.L.H., Columbia University, The University of Melbourne, Austin Health and Royal Melbourne Hospital, Australia Centre for Clinical Translation (M.R.J.), Imperial College London, Charing Cross Hospital Campus, The Florey Institute of Neuroscience
Michael R JohnsonDuke University School of Medicine (R.S.D., NC Institute for Genomic Medicine (E.L.H., Columbia University, The University of Melbourne, Austin Health and Royal Melbourne Hospital, Australia Centre for Clinical Translation (M.R.J.), Imperial College London, Charing Cross Hospital Campus, The Florey Institute of Neuroscience
David B GoldsteinDuke University School of Medicine (R.S.D., NC Institute for Genomic Medicine (E.L.H., Columbia University, The University of Melbourne, Austin Health and Royal Melbourne Hospital, Australia Centre for Clinical Translation (M.R.J.), Imperial College London, Charing Cross Hospital Campus, The Florey Institute of Neuroscience
David B GoldsteinDuke University School of Medicine (R.S.D., NC Institute for Genomic Medicine (E.L.H., Columbia University, The University of Melbourne, Austin Health and Royal Melbourne Hospital, Australia Centre for Clinical Translation (M.R.J.), Imperial College London, Charing Cross Hospital Campus, The Florey Institute of Neuroscience
  • 1 - 4

Datasets

Release 1.2