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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Detalles Bibliográficos
Autores principales: Park, Jun Young, Joo, Kwangsic, Woo, Se Joon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472957/
https://www.ncbi.nlm.nih.gov/pubmed/32973440
http://dx.doi.org/10.3389/fnins.2020.00892

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472957/
https://www.ncbi.nlm.nih.gov/pubmed/32973440
http://dx.doi.org/10.3389/fnins.2020.00892

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