Associated Papers
De Novo GRID2 Variant as a Cause of Ataxia with Oculomotor Apraxia and Alpha-Fetoprotein Elevation.
Sartorelli J et al.
Cerebellum (london, England), 2024
A heterozygous GRID2 mutation in autosomal dominant cerebellar ataxia.
Koh K et al.
Human Genome Variation, 2022
Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature.
Ceylan AC et al.
Acta Neurologica Belgica, 2021
Exome sequencing in the clinical diagnosis of sporadic or familial cerebellar ataxia.
Fogel BL et al.
Jama Neurology, 2014
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