Molecular genetics of congenital myotonic dystrophy
Myotonic Dystrophy type 1 (DM1) is a neuromuscular disease showing strong genetic anticipation, and is caused by the expansion of a CTG repeat tract in the 3′-UTR of the DMPK gene. Congenital Myotonic Dystrophy (CDM1) represents the most severe form of the disease, with prenatal onset, symptoms dist...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2019-12-01
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| Sarja: | Neurobiology of Disease |
| Aiheet: | |
| Linkit: | http://www.sciencedirect.com/science/article/pii/S0969996119302013 |
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