ロード中...
The molecular basis of HEXA mRNA deficiency caused by the most common Tay-Sachs disease mutation.
Tay-Sachs disease (TSD) is a catastrophic neurodegenerative disorder caused by mutations in the HEXA gene. The most common TSD allele worldwide contains a 4-bp insertion in exon 11 that produces a downstream premature termination codon. Despite normal transcription of this allele, HEXA mRNA is sever...
保存先:
| 主要な著者: | , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
1995
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1801160/ https://ncbi.nlm.nih.gov/pubmed/7887427 |
| 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!
|