Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion.
| Image |  |
|---|---|
| Description | scientific article published on 14 August 2014 |
| Author/s |
author: Frauke Coppieters Christian Van Nechel Elfride De Baere |
| Publication date | August 14, 2014 |
| Language | English |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |