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pro vyhledávání: '"Edgar(Ned) A Buttner"'
Autor:
XIN WANG, Limin Hao, Taixiang Saur, Katelyn JOYAL, Ying Zhao, Desheng Zhai, Jie Li, Mochtar Pribadi, Giovanni Coppola, Bruce M Cohen, Edgar(Ned) A Buttner
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 9 (2016)
An abnormally expanded GGGGCC repeat in C9ORF72 is the most frequent causal mutation associated with amyotrophic lateral sclerosis (ALS) frontotemporal lobar degeneration (FTLD). Both gain-of-function (gf) and loss-of-function (lf) mechanisms have be
Externí odkaz:
https://doaj.org/article/3e8f410271b548a090223a6ddf7f7562
