ロード中...
Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
In a previous study we identified 14 cases with Duchenne muscular dystrophy (DMD) or its milder variant, Becker muscular dystrophy (BMD), with a deletion of exons 3-7, a deletion that would be expected to shift the translational reading frame of the mRNA and give a severe phenotype. We have examined...
保存先:
| 主要な著者: | , , , , , , , , |
|---|---|
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
1992
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1682710/ https://ncbi.nlm.nih.gov/pubmed/1496988 |
| 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!
|