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Modifiers of CAG/CTG Repeat Instability: Insights from Mammalian Models
At fifteen different genomic locations, the expansion of a CAG/CTG repeat causes a neurodegenerative or neuromuscular disease, the most common being Huntington’s disease and myotonic dystrophy type 1. These disorders are characterized by germline and somatic instability of the causative CAG/CTG repe...
Uloženo v:
| Vydáno v: | J Huntingtons Dis |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
IOS Press
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7990408/ https://ncbi.nlm.nih.gov/pubmed/33579861 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/JHD-200426 |
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