Publications


SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases.
Eur J Hum Genet 2016 Jul 2;24(7):1016-21. Epub 2015 Dec 2.
Neurogenetics of Motion Laboratory, Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Québec, Canada.


Neuropathologic features of pontocerebellar hypoplasia type 6.
J Neuropathol Exp Neurol 2014 Nov;73(11):1009-25
From the Calgary Laboratory Services (JTJ) and Alberta Children's Hospital Foundation Research Institute for Child and Maternal Health, Department of Medical Genetics (AMI), University of Calgary, Calgary, Alberta; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario (ACS, MRV, FCC, DEB, JMichaud, KMB); and McGill University and Genome Quebec Innovation Center, Montreal, Quebec (JAS, JMajewski), Canada; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, Washington (RFH, RAD); and Department of Neurological Surgery, University of Washington, Seattle, Washington (RFH).




OF