Myotonic Dystrophy Type 2 Caused by a CCTG Expansion in Intron 1 of ZNF9

1.

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

2.

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

3.

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

4.

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

5.

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