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Eye Movement Abnormalities in Joubert Syndrome
PURPOSE: Joubert syndrome is a genetic disorder characterized by hypoplasia of the midline cerebellum and deficiency of crossed connections between neural structures in the brain stem that control eye movements. The goal of the study was to quantify the eye movement abnormalities that occur in Joube...
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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3919872/ https://ncbi.nlm.nih.gov/pubmed/19443711 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.08-3299 |
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