Variability of Creatine Metabolism Genes in Children with Autism Spectrum Disorder

by Jessie M. Cameron, Valeriy Levandovskiy, Wendy Roberts, Evdokia Anagnostou, Stephen Scherer, Alvin Loh, Andreas Schulze
Published 2017-07-01

Novel recessive mutations in COQ4 cause severe infantile cardiomyopathy and encephalopathy associated with CoQ10 deficiency

by Neal Sondheimer, Stacy Hewson, Jessie M. Cameron, Gino R. Somers, Jane Dunning Broadbent, Marcello Ziosi, Catarina Maria Quinzii, Ali B. Naini
Published 2017-09-01

Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy.

by Karen M Vernau, Jonathan A Runstadler, Emily A Brown, Jessie M Cameron, Heather J Huson, Robert J Higgins, Cameron Ackerley, Beverly K Sturges, Peter J Dickinson, Birgit Puschner, Cecilia Giulivi, G Diane Shelton, Brian H Robinson, Salvatore DiMauro, Andrew W Bollen, Danika L Bannasch
Published 2013-01-01