Related references
Note: Only part of the references are listed.
Article
Genetics & Heredity
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
Alexander J. Abrams et al.
NATURE GENETICS (2015)
Article
Clinical Neurology
The role of the cerebellum in the pathogenesis of cortical myoclonus
Christos Ganos et al.
MOVEMENT DISORDERS (2014)
Article
Biotechnology & Applied Microbiology
Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system
Tatjana Haitina et al.
GENOMICS (2006)