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Heritability of saccadic eye movements in spinocerebellar ataxia type 2: insights into an endophenotype marker

BACKGROUND: Saccade slowing has been proposed as endophenotype marker in Spinocerebellar Ataxia type 2 (SCA2), nevertheless the heritability of this trait has not been properly demonstrated. Thus the present paper was aimed to assess the heritability of different saccadic parameters in SCA2. METHODS...

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Detalhes bibliográficos
Publicado no:Cerebellum Ataxias
Main Authors: Rodríguez-Labrada, Roberto, Vázquez-Mojena, Yaimeé, Canales-Ochoa, Nalia, Medrano-Montero, Jacqueline, Velázquez-Pérez, Luis
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5738191/
https://ncbi.nlm.nih.gov/pubmed/29276612
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40673-017-0078-2
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