ロード中...

In vitro expansion of GGC:GCC repeats: identification of the preferred strand of expansion.

The human fragile-X syndrome, a major cause of inherited mental retardation, is associated with expansion of the trinucleotide repeat GGC:GCC. Repetitive sequences in DNA are subject to slippage during catalysis by DNA polymerases. We characterized the extent of slippage of synthetic GGC:GCC repeats...

詳細記述

保存先:
書誌詳細
主要な著者: Ji, J, Clegg, N J, Peterson, K R, Jackson, A L, Laird, C D, Loeb, L A
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/PMC146016/
https://ncbi.nlm.nih.gov/pubmed/8759019
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!