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Mouse Models of Human CAG Repeat Disorders
Expansions of CAG trinucleotide repeats encoding glutamine have been found to be the causative mutations of seven human neurodegenerative diseases. Similarities in the clinical, genetic, and molecular features of these disorders suggest they share a common mechanism of pathogenesis. Recent progress...
Shranjeno v:
| izdano v: | Brain Pathol |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Blackwell Publishing Ltd
2008
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8098257/ https://ncbi.nlm.nih.gov/pubmed/9217978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1750-3639.1997.tb00896.x |
| Oznake: |
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