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In Vitro Expansion of CAG, CAA, and Mixed CAG/CAA Repeats
Polyglutamine diseases, including Huntington’s disease and a number of spinocerebellar ataxias, are caused by expanded CAG repeats that are located in translated sequences of individual, functionally-unrelated genes. Only mutant proteins containing polyglutamine expansions have long been thought to...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4581269/ https://ncbi.nlm.nih.gov/pubmed/26270660 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms160818741 |
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