ロード中...

Aminoglycoside-induced mutation suppression (stop codon readthrough) as a therapeutic strategy for Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is the most common, lethal, X-linked genetic disease, affecting 1 in 3500 newborn males. It is caused by mutations in the DMD gene. Owing to the large size of the gene, the mutation rate in both germline and somatic cells is very high. Nearly 13–15% of DMD cases are...

詳細記述

保存先:
書誌詳細
主要な著者: Malik, Vinod, Rodino-Klapac, Louise R., Viollet, Laurence, Mendell, Jerry R.
フォーマット: Artigo
言語:Inglês
出版事項: SAGE Publications 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3002642/
https://ncbi.nlm.nih.gov/pubmed/21179598
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1756285610388693
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!