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Single-nucleus RNA-seq identifies Huntington disease astrocyte states
Huntington Disease (HD) is an inherited movement disorder caused by expanded CAG repeats in the Huntingtin gene. We have used single nucleus RNASeq (snRNASeq) to uncover cellular phenotypes that change in the disease, investigating single cell gene expression in cingulate cortex of patients with HD...
Autores principales: | Al-Dalahmah, Osama, Sosunov, Alexander A., Shaik, A., Ofori, Kenneth, Liu, Yang, Vonsattel, Jean Paul, Adorjan, Istvan, Menon, Vilas, Goldman, James E. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029580/ https://www.ncbi.nlm.nih.gov/pubmed/32070434 http://dx.doi.org/10.1186/s40478-020-0880-6 |
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