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Anti-sense DNA d(GGCCCC)(n) expansions in C9ORF72 form i-motifs and protonated hairpins
The G(4)C(2) hexanucleotide repeat expansion mutation (HREM) in C9ORF72, represents the most common mutation associated with amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). Three main disease mechanisms have been proposed to date: C9ORF72 haploinsufficiency, RNA tox...
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| Publicado no: | Sci Rep |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4668579/ https://ncbi.nlm.nih.gov/pubmed/26632347 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep17944 |
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