Van Schil, Kristof
Meire, Françoise
Karlstetter, Marcus
Bauwens, Miriam
Verdin, Hannah
Coppieters, Frauke
Scheiffert, Eva
Van Nechel, Christian
Langmann, Thomas
Deconinck, Nicolas
De Baere, Elfride
This article is maintained by: Elsevier
Article Title: Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/gim.2014.95
Content Type: article
Copyright: © 2015, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics