Confirmation of the Type 2 Myotonic Dystrophy (CCTG)n Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect

✍ Scribed by Linda L. Bachinski; Bjarne Udd; Giovanni Meola; Valeria Sansone; Guillaume Bassez; Bruno Eymard; Charles A. Thornton; Richard T. Moxley; Peter S. Harper; Mark T. Rogers; Karin Jurkat-Rott; Frank Lehmann-Horn; Thomas Wieser; Josep Gamez; Carmen Navarro; Armand Bottani; Andre Kohler; Mark D. Shriver; Riitta Sallinen; Maija Wessman; Shanxiang Zhang; Fred A. Wright; Ralf Krahe

• Book ID: 117854302
• Publisher: American Society of Human Genetics
• Year: 2003
• Tongue: English
• Weight: 743 KB
• Volume: 73
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/378566