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Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review

Spinocerebellar ataxia (SCA) is a part of the cerebellar neurodegenerative disease group that is diverse in genetics and phenotypes. It usually shows autosomal dominant inheritance. SCAs, always together with the cerebellar degeneration, may exhibit clinical deficits in brainstem or eye, especially...

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Publicado en:Front Neurosci
Main Authors: Park, Jun Young, Joo, Kwangsic, Woo, Se Joon
Formato: Artigo
Idioma:Inglês
Publicado: Frontiers Media S.A. 2020
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7472957/
https://ncbi.nlm.nih.gov/pubmed/32973440
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2020.00892
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