Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion. (Q49052576)
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scientific article published on 14 August 2014
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
Statements
Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion (English)
Christian Van Nechel
Kristof Van Schil
Françoise Meire
Marcus Karlstetter
Miriam Bauwens
Hannah Verdin
Eva Scheiffert
Thomas Langmann
Nicolas Deconinck
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