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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Research Center of Neurology
2017-02-01
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| Σειρά: | Анналы клинической и экспериментальной неврологии |
| Θέματα: | |
| Διαθέσιμο Online: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/269/178 |
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