Myotonic Dystrophy Type 2 Caused by a CCTG

Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9 by Christina L. Liquori, Kenneth Ricker, Melinda L. Moseley, Jennifer F. Jacobsen, Wolfram Kress, Susan L. Naylor, John W. Day, and Laura P. W. Ranum Science Volume 293(5531):864-867 August 3, 2001 Published by AAAS

Figure 1 Expanded CL3N58 allele found in DM2 patients. Christina L. Liquori et al. Science 2001;293:864-867 Published by AAAS

Figure 2 Analysis of DM2-affected and normal alleles. Christina L. Liquori et al. Science 2001;293:864-867 Published by AAAS

Figure 3 Instability of the DM2 expansion. Christina L. Liquori et al. Science 2001;293:864-867 Published by AAAS

Figure 4 RNA in situ hybridization of the expansion. Christina L. Liquori et al. Science 2001;293:864-867 Published by AAAS