Dysfunction of the Cerebral Glucose Transporter SLC45A1 in Individuals with Intellectual Disability and Epilepsy

Myriam Srour(Montreal Children's Hospital), Jacques L. Michaud(Centre Hospitalier Universitaire Sainte-Justine)
The American Journal of Human Genetics
April 20, 2017
10.1016/j.ajhg.2017.03.009
Cited by 40

Related Papers

Developmental trajectory of oligodendrocyte progenitor cells in the human brain revealed by single cell RNA sequencing
|Glia|2020|75
Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG)
|Journal of Medical Genetics|2023|57
Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals
|Genetics in Medicine|2022|39
Age-related injury responses of human oligodendrocytes to metabolic insults: link to BCL-2 and autophagy pathways
|Communications Biology|2021|37
Expanding the phenotypic and molecular spectrum of RNA polymerase III–related leukodystrophy
|Neurology Genetics|2020|36