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 Lehmann-Horn, Thomas Wieser, Josep Gamez, Carmen Navarro, Armand Bottani, Andre Kohler, Mark D. Shriver, Riitta Sallinen, Maija WessmanShanxiang Zhang, Fred A. Wright, Ralf Krahe

Research output: Contribution to journal › Article › peer-review

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