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
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 LehmaVolume:
73
Year:
2003
Language:
english
DOI:
10.1086/378566
File:
PDF, 743 KB
english, 2003