Erratum to: Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

Readthrough of nonsense mutations in Ret

Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model

✍ Cornelia Brendel; Valery Belakhov; Hauke Werner; Eike Wegener; Jutta Gärtner; Ig 📂 Article 📅 2010 🏛 Springer 🌐 English ⚖ 763 KB

Thirty-five percent of patients with Rett syndrome carry nonsense mutations in the __MECP2__ gene. We have recently shown in transfected HeLa cells that readthrough of nonsense mutations in the __MECP2__ gene can be achieved by treatment with gentamicin and geneticin. This study was performed to tes