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Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion.
scientific article published on 14 August 2014
Author/s
author: Frauke Coppieters, Elfride De Baere, Christian Van Nechel
Work details
Publication date
August 14, 2014
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Language
English
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