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Autor:
Neill R. Graff-Radford, Sergio Sebastian Pineda, Ronald C. Petersen, Julio Mantero, Bjorn Oskarsson, Mariely DeJesus-Hernandez, Jaimin S. Shah, Veronique V. Belzil, Melissa E. Murray, Erica Engelberg-Cook, Michael DeTure, Brent Eugene Fitzwalter, Rosa Rademakers, Bradley F. Boeve, Hyeseung Lee, Luc Pregent, Dennis W. Dickson, Mahammad E Gardashli, Shahin Mohammadi, David S. Knopman, Manolis Kellis, Cyril Pottier, Marka van Blitterswijk, Keith A. Josephs, Myriam Heiman
Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are two devastating and fatal neurodegenerative conditions. While distinct, they share many clinical, genetic, and pathological characteristics1, and both show selective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0a3a52304aac71720fc15a8376c6619d
https://doi.org/10.1101/2021.07.07.451374
https://doi.org/10.1101/2021.07.07.451374
