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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...

詳細記述

保存先:
書誌詳細
出版年:Front Neurosci
主要な著者: Park, Jun Young, Joo, Kwangsic, Woo, Se Joon
フォーマット: Artigo
言語:Inglês
出版事項: Frontiers Media S.A. 2020
主題:
オンライン・アクセス: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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