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...
Sábháilte in:
| Príomhchruthaitheoirí: | , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe / Cruthaithe: |
Research Center of Neurology
2017-02-01
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| Sraith: | Анналы клинической и экспериментальной неврологии |
| Ábhair: | |
| Rochtain ar líne: | https://annaly-nevrologii.com/journal/pathID/article/viewFile/269/178 |
| Clibeanna: |
Níl clibeanna ann, Bí ar an gcéad duine le clib a chur leis an taifead seo!
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