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Somatic mutation that affects transcription factor binding upstream of CD55 in the temporal cortex of a late-onset Alzheimer disease patient
Alzheimer’s disease (AD) is the most common neurodegenerative disease worldwide. Familial cases suggest genetic components; however, monogenetic causes are few, and the vast majority of incidences have unknown cause. Sequencing efforts have focused on germline mutations, but improved technology has...
Autores principales: | Helgadottir, Hafdis T, Lundin, Pär, Wallén Arzt, Emelie, Lindström, Anna-Karin, Graff, Caroline, Eriksson, Maria |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6688063/ https://www.ncbi.nlm.nih.gov/pubmed/31216356 http://dx.doi.org/10.1093/hmg/ddz085 |
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