← Evidence map

ArticleThe Journal of clinical investigation1997

Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.

N Shiga et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

49 papers cite it

1997
…
2006
2007
2008
2009
2010
2011
2012
2013
2014
2015
2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 9410897