Myotonic dystrophy type 2
Myotonic dystrophy, type 2 (DM2) is an autosomal dominantdisorder caused by expansion of the CCTG repeats in the zinkfinger protein-9 gene (ZNF9). It has been clinically reported inthe middle 1990th. DM2 is less frequent than classic DM1,yet is relatively common, mostly in Europeans. Like DM1,DM2 is...
| Published in: | Анналы клинической и экспериментальной неврологии |
|---|---|
| Main Authors: | , |
| Format: | Article |
| Language: | English |
| Published: |
Research Center of Neurology
2017-02-01
|
| Subjects: | |
| Online Access: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/269/178 |