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C9ORF72 transcription in a frontotemporal dementia case with two expanded alleles
Discovery of intronic hexanucleotide repeat expansions of the C9ORF72 gene in a significant proportion of patients with amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD)(1,2) was an important step for research into these disorders. The C9ORF72 genetic variant is more common than...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Lippincott Williams & Wilkins
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3812108/ https://ncbi.nlm.nih.gov/pubmed/24107864 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000435295.41974.2e |
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