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Paper Details

Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy.
Mov Disord Clin Pract
7
2020
Cerebellar Atrophy, Cerebellar atrophy, Channelopathies, Genetic Ataxias, Genetic ataxias, Rare, Rare Genetic Disease, Rare Genetic Diseases, cerebellar atrophy, channelopathies, genetic ataxias, neurological disorders, novel genes, participants
Author NameAffiliation
Taila HartleyChildren's Hospital of Eastern Ontario Research Institute University of Ottawa Ottawa Ontario Canada.
Mark A TarnopolskyDepartment of Paediatrics McMaster University Medical Centre Hamilton Ontario Canada.
Guy A RouleauDepartment of Neurology and Neurosurgery McGill University, Montreal Neurological Institute Montreal Qubec Canada.
Guy A RouleauDepartment of Neurology and Neurosurgery McGill University, Montreal Neurological Institute Montreal Qubec Canada.
Kym M BoycottChildren's Hospital of Eastern Ontario Research Institute University of Ottawa Ottawa Ontario Canada.
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Release 1.2