ロード中...
Midbrain atrophy related to parkinsonism in a non-coding repeat expansion disorder: five cases of spinocerebellar ataxia type 31 with nigrostriatal dopaminergic dysfunction
BACKGROUND: Spinocerebellar ataxia type 31 (SCA31) is caused by non-coding pentanucleotide repeat expansions in the BEAN1 gene. Clinically, SCA31 is characterized by late adult-onset, pure cerebellar ataxia. To explore the association between parkinsonism and SCA31, five patients with SCA31 with con...
保存先:
| 出版年: | Cerebellum Ataxias |
|---|---|
| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2021
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8010976/ https://ncbi.nlm.nih.gov/pubmed/33785066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s40673-021-00134-4 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|