Eye-tracking-aided characterization of saccades and antisaccades in SYNE1 ataxia patients
SYNE1 ataxia is an autosomal recessive hereditary condition, the main characteristic features of which are gait and limb ataxia and cerebellar dysarthria. Reports have revealed that the clinical phenotype of SYNE1 ataxia is more complex than the first published cases with pure cerebellar signs indic...
Elmentve itt :
| Szerzők: | |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
2021
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| Sorozat: | BMC NEUROSCIENCE
22 No. 1 |
| doi: | 10.1186/s12868-021-00612-9 |
| mtmt: | 31853117 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/20869 |