Open AccessLoss of Stathmin-2, a hallmark of TDP-43-associated ALS, causes motor neuropathy
Author(s) -
Kelsey L. Krus,
Amy Strickland,
Yurie Yamada,
Laura DeVault,
Robert E. Schmidt,
A. Joseph Bloom,
Jeffrey Milbrandt,
Aaron DiAntonio
Publication year - 2022
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2022.111001
Subject(s) - amyotrophic lateral sclerosis , denervation , neuroscience , pathogenesis , neuromuscular junction , spinal cord , axon , conditional gene knockout , motor neuron , knockout mouse , medicine , biology , pathology , anatomy , disease , biochemistry , receptor , gene , phenotype
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