ロード中...
Expansion of polyglutamine repeat in huntingtin leads to abnormal protein interactions involving calmodulin.
Huntington's disease (HD) is an inherited neurodegenerative disorder associated with expansion of a CAG repeat in the IT15 gene. The IT15 gene is translated to a protein product termed huntingtin that contains a polyglutamine (polyGln) tract. Recent investigations indicate that the cause of HD...
保存先:
| 主要な著者: | , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
1996
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC39402/ https://ncbi.nlm.nih.gov/pubmed/8643525 |
| 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!
|