A carregar...

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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Malik, Vinod, Rodino-Klapac, Louise R., Viollet, Laurence, Mendell, Jerry R.
Formato: Artigo
Idioma:Inglês
Publicado em: SAGE Publications 2010
Assuntos:
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!