ロード中...
A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder characterized by motor disturbance, cognitive loss, and psychiatric manifestations. The disease is associated with a CAG trinucleotide-repeat expansion in the Huntington gene (IT15) on chromosome 4p16.3. One family with a hi...
保存先:
| 主要な著者: | , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
1998
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1377554/ https://ncbi.nlm.nih.gov/pubmed/9792871 |
| 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!
|