Confirmation of the Type 2 Myotonic Dystrophy (CCTG) Expansion Mutation in Patients with Proximal Myotonic Myopathy/Proximal Myotonic Dystrophy of Different European Origins: A Single Shared Haplotype Indicates an Ancestral Founder Effect
The American Journal of Human Genetics2003Vol. 73(4), pp. 835–848
Citations Over TimeTop 10% of 2003 papers
Linda L. Bachinski, Bjarne Udd, G. Meola, Valeria Sansone, Guillaume Bassez, B. Eymard, Charles A. Thornton, Richard T. Moxley, Peter S. Harper, Mark T. Rogers, Karin Jurkat‐Rott, Frank Lehmann‐Horn, Thomas Wieser, Josep Gámez, Carmen Navarro, Armand Bottani, André Köhler, Mark D. Shriver, Riitta Sallinen, Maija Wessman, Shanxiang Zhang, Fred A. Wright, Ralf Krahe
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