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Recognition of c9orf72 Mutant RNA by Single-Stranded Silencing RNAs
Mutations within the chromosome 9 open reading frame 72 (c9orf72) gene are associated with both familial amyotrophic lateral sclerosis and frontotemporal dementia. The mutation leads to an expanded GGGGCC hexanucleotide repeat within the first intron of c9orf72 and an expanded CCCCGG repeat within a...
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| Publicado no: | Nucleic Acid Ther |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Mary Ann Liebert, Inc.
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5372765/ https://ncbi.nlm.nih.gov/pubmed/28005462 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/nat.2016.0655 |
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