New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2)

✍ Scribed by R Sallinen; A Vihola; L.L Bachinski; K Huoponen; H Haapasalo; P Hackman; S Zhang; M Sirito; H Kalimo; G Meola; N Horelli-Kuitunen; M Wessman; R Krahe; B Udd

• Book ID: 116792158
• Publisher: Elsevier Science
• Year: 2004
• Tongue: English
• Weight: 280 KB
• Volume: 14
• Category: Article
• ISSN: 0960-8966
• DOI: 10.1016/j.nmd.2004.01.002