Erratum: Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011))

Irune Guerra San Juan; Leslie A. Nash; Kevin S. Smith; Marcel F. Leyton-Jaimes; Menglu Qian; Joseph R. Klim; Francesco Limone; Alexander B. Dorr; Alexander Couto; Greta Pintacuda; Brian J. Joseph; D. Eric Whisenant; Caroline Noble; Veronika Melnik; Deirdre Potter; Amie Holmes; Aaron Burberry; Matthijs Verhage; Kevin Eggan

doi:10.1016/j.neuron.2022.11.003

Erratum: Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011))

Irune Guerra San Juan, Leslie A. Nash, Kevin S. Smith, Marcel F. Leyton-Jaimes, Menglu Qian, Joseph R. Klim, Francesco Limone, Alexander B. Dorr, Alexander Couto, Greta Pintacuda, Brian J. Joseph, D. Eric Whisenant, Caroline Noble, Veronika Melnik, Deirdre Potter, Amie Holmes, Aaron Burberry, Matthijs Verhage, Kevin Eggan

Department of Physiology and Cell Biology

Research output: Contribution to journal › Comment/debate

Abstract

(Neuron 110, 1671–1688; May 18, 2022) It was brought to our attention that there is a clerical mistake in one of the panels of Figure 1 (Figure 1E) in our recent publication. The representative blots for the CNS Stmn2 protein levels in the F₂ generation of Stmn2 mutants included an incorrect duplicated blot for the GAPDH loading control in the brain samples. We have corrected this error and replaced the figure online with one that includes the correct blot for the GAPDH loading control for those samples. We would like to profoundly apologize to the readers for the oversight and honest mistake.[Formula

Original language	English
Pages (from-to)	4031
Number of pages	1
Journal	Neuron
Volume	110
Issue number	23
DOIs	https://doi.org/10.1016/j.neuron.2022.11.003
State	Published - 7 Dec 2022

ASJC Scopus subject areas

General Neuroscience

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San Juan, I. G., Nash, L. A., Smith, K. S., Leyton-Jaimes, M. F., Qian, M., Klim, J. R., Limone, F., Dorr, A. B., Couto, A., Pintacuda, G., Joseph, B. J., Whisenant, D. E., Noble, C., Melnik, V., Potter, D., Holmes, A., Burberry, A., Verhage, M., & Eggan, K. (2022). Erratum: Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011)). Neuron, 110(23), 4031. https://doi.org/10.1016/j.neuron.2022.11.003

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title = "Erratum: Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011))",

abstract = "(Neuron 110, 1671–1688; May 18, 2022) It was brought to our attention that there is a clerical mistake in one of the panels of Figure 1 (Figure 1E) in our recent publication. The representative blots for the CNS Stmn2 protein levels in the F2 generation of Stmn2 mutants included an incorrect duplicated blot for the GAPDH loading control in the brain samples. We have corrected this error and replaced the figure online with one that includes the correct blot for the GAPDH loading control for those samples. We would like to profoundly apologize to the readers for the oversight and honest mistake.[Formula",

author = "{San Juan}, {Irune Guerra} and Nash, {Leslie A.} and Smith, {Kevin S.} and Leyton-Jaimes, {Marcel F.} and Menglu Qian and Klim, {Joseph R.} and Francesco Limone and Dorr, {Alexander B.} and Alexander Couto and Greta Pintacuda and Joseph, {Brian J.} and Whisenant, {D. Eric} and Caroline Noble and Veronika Melnik and Deirdre Potter and Amie Holmes and Aaron Burberry and Matthijs Verhage and Kevin Eggan",

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year = "2022",

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doi = "10.1016/j.neuron.2022.11.003",

language = "English",

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San Juan, IG, Nash, LA, Smith, KS, Leyton-Jaimes, MF, Qian, M, Klim, JR, Limone, F, Dorr, AB, Couto, A, Pintacuda, G, Joseph, BJ, Whisenant, DE, Noble, C, Melnik, V, Potter, D, Holmes, A, Burberry, A, Verhage, M & Eggan, K 2022, 'Erratum: Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011))', Neuron, vol. 110, no. 23, pp. 4031. https://doi.org/10.1016/j.neuron.2022.11.003

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T2 - Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011))

AU - San Juan, Irune Guerra

AU - Nash, Leslie A.

AU - Smith, Kevin S.

AU - Leyton-Jaimes, Marcel F.

AU - Qian, Menglu

AU - Klim, Joseph R.

AU - Limone, Francesco

AU - Dorr, Alexander B.

AU - Couto, Alexander

AU - Pintacuda, Greta

AU - Joseph, Brian J.

AU - Whisenant, D. Eric

AU - Noble, Caroline

AU - Melnik, Veronika

AU - Potter, Deirdre

AU - Holmes, Amie

AU - Burberry, Aaron

AU - Verhage, Matthijs

AU - Eggan, Kevin

PY - 2022/12/7

Y1 - 2022/12/7

N2 - (Neuron 110, 1671–1688; May 18, 2022) It was brought to our attention that there is a clerical mistake in one of the panels of Figure 1 (Figure 1E) in our recent publication. The representative blots for the CNS Stmn2 protein levels in the F2 generation of Stmn2 mutants included an incorrect duplicated blot for the GAPDH loading control in the brain samples. We have corrected this error and replaced the figure online with one that includes the correct blot for the GAPDH loading control for those samples. We would like to profoundly apologize to the readers for the oversight and honest mistake.[Formula

AB - (Neuron 110, 1671–1688; May 18, 2022) It was brought to our attention that there is a clerical mistake in one of the panels of Figure 1 (Figure 1E) in our recent publication. The representative blots for the CNS Stmn2 protein levels in the F2 generation of Stmn2 mutants included an incorrect duplicated blot for the GAPDH loading control in the brain samples. We have corrected this error and replaced the figure online with one that includes the correct blot for the GAPDH loading control for those samples. We would like to profoundly apologize to the readers for the oversight and honest mistake.[Formula

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JO - Neuron

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Erratum: Loss of mouse Stmn2 function causes motor neuropathy (Neuron (2022) 110(10) (1671–1688.e6), (S0896627322001763), (10.1016/j.neuron.2022.02.011))

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