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pro vyhledávání: '"C. D. Clelland"'
Autor:
S. E. Salomonsson, A. M. Maltos, K. Gill, O. Aladesuyi Arogundade, K. A. Brown, A. Sachdev, M. Sckaff, K. J. K. Lam, I. J. Fisher, R. S. Chouhan, V. S. Van Laar, C. B. Marley, I. McLaughlin, K. S. Bankiewicz, Y.-C. Tsai, B. R. Conklin, C. D. Clelland
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract A repeat expansion mutation in the C9orf72 gene is the leading known genetic cause of FTD and ALS. The C9orf72-ALS/FTD field has been plagued by a lack of reliable tools to monitor this genomic locus and its RNA and protein products. We have
Externí odkaz:
https://doaj.org/article/782f10f759d84e6aa3c479b903db9782
