(CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients

G. Novelli, M. Gennarelli, E. Menegazzo, M.L. Mostacciuolo, A. Pizzuti, C. Fattorini, D. Tessarolo, G. Tomelleri, M. Giacanelli, G.A. Danieli, N. Rizzuto, C.T. Caskey, C. Angelini, B. Dallapiccola
  • Biochemical Medicine and Metabolic Biology, August 1993, Elsevier
  • DOI: 10.1006/bmmb.1993.1049

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The following have contributed to this page: Prof Corrado Angelini