Characteristic Eye Movements in Ataxia-Telangiectasia-Like Disorder: An Explanatory Hypothesis

OBJECTIVE: To investigate cerebellar dysfunctions and quantitatively characterize specific oculomotor changes in ataxia-telangiectasia-like disorder (ATLD), a rare autosomal recessive disease caused by mutations in the MRE11 gene. Additionally, to further elucidate the pathophysiology of cerebellar...

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Detalles Bibliográficos
Autores principales: Federighi, Pamela, Ramat, Stefano, Rosini, Francesca, Pretegiani, Elena, Federico, Antonio, Rufa, Alessandra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684103/
https://www.ncbi.nlm.nih.gov/pubmed/29170652
http://dx.doi.org/10.3389/fneur.2017.00596

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5684103/
https://www.ncbi.nlm.nih.gov/pubmed/29170652
http://dx.doi.org/10.3389/fneur.2017.00596

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