Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family

✍ Scribed by Ginjaar, Ieke B; Kneppers, Alexander LJ; v d Meulen, Jan-Douwe M; Anderson, Louise VB; Bremmer-Bout, Mattie; van Deutekom, Judith CT; Weegenaar, Jitske; den Dunnen, Johan T; Bakker, Egbert

• Book ID: 110025029
• Publisher: Nature Publishing Group
• Year: 2000
• Tongue: English
• Weight: 413 KB
• Volume: 8
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/sj.ejhg.5200535