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Forward Genetic Screen in
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Xin Wang
,
Limin Hao
,
Taixiang Saur
+8 more
· 2016 · Frontiers in molecular neuroscience · Frontiers
· added 2026-04-24
Xin Wang
,
Limin Hao
,
Taixiang Saur
,
Katelyn Joyal
,
Ying Zhao
,
Desheng Zhai
,
Jie Li
,
Mochtar Pribadi
,
Giovanni Coppola
,
Bruce M Cohen
,
Edgar A Buttner
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An abnormally expanded GGGGCC repeat in C9ORF72 is the most frequent causal mutation associated with amyotrophic lateral sclerosis (ALS)/frontotemporal lobar degeneration (FTLD). Both
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DOI:
10.3389/fnmol.2016.00113
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