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. 2020 Feb 14;29(6):1056. doi: 10.1093/hmg/ddaa012

Smcr8 deficiency disrupts axonal transport-dependent lysosomal function and promotes axonal swellings and gain of toxicity in C9ALS/FTD mouse models

Chen Liang 1,2, Qiang Shao 1, Wei Zhang 1, Mei Yang 1, Qing Chang 1, Rong Chen 3, Jian-Fu Chen 1,
PMCID: PMC7158374  PMID: 32057072

Since article was originally published online, some minor corrections which had been missed at the proof stage (due to OUP error) have since been updated: 1) In Fig, 5F, WT, and Smcr8-/- have been added into the labels, and also *, n.s. in the notes; 2) In Fig. 9C, GR has been amended to GP following a re-calculation, because the authors found that previous GR antibody recognizes non-specific autofluorescent proteins. The modifications did not change the conclusions and interpretation of the results.


Articles from Human Molecular Genetics are provided here courtesy of Oxford University Press

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