Two common mutations (p.Gln832X and c.663+1G>C) account for about a third of the DYSF mutations in Korean patients with dysferlinopathy

✍ Scribed by Young-Eun Park; Hyang-Sook Kim; Chang-Hoon Lee; Tai-Seung Nam; Young-Chul Choi; Dae-Seong Kim

• Book ID: 116795237
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 225 KB
• Volume: 22
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2011.12.007