Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123)

Luis Carlos Tábara; Fatema Al-Salmi; Reza Maroofian; Amna Mohammed Al-Futaisi; Fathiya Al-Murshedi; Joanna Kennedy; Jacob O. Day; Thomas Courtin; Aisha Al-Khayat; Hamid Galedari; Neda Mazaheri; Margherita Protasoni; Mark Johnson; Joseph S. Leslie; Claire G. Salter; Lettie E. Rawlins; James Fasham; Almundher Al-Maawali; Nikol Voutsina; Perrine Charles; Laura Harrold; Boris Keren; Edmund R.S. Kunji; Barbara Vona; Gholamreza Jelodar; Alireza Sedaghat; Gholamreza Shariati; Henry Houlden; Andrew H. Crosby; Julien Prudent; Emma L. Baple

doi:10.1093/brain/awac254

Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123)

Luis Carlos Tábara, Fatema Al-Salmi, Reza Maroofian, Amna Mohammed Al-Futaisi, Fathiya Al-Murshedi, Joanna Kennedy, Jacob O. Day, Thomas Courtin, Aisha Al-Khayat, Hamid Galedari, Neda Mazaheri, Margherita Protasoni, Mark Johnson, Joseph S. Leslie, Claire G. Salter, Lettie E. Rawlins, James Fasham, Almundher Al-Maawali, Nikol Voutsina, Perrine CharlesLaura Harrold, Boris Keren, Edmund R.S. Kunji, Barbara Vona, Gholamreza Jelodar, Alireza Sedaghat, Gholamreza Shariati, Henry Houlden, Andrew H. Crosby, Julien Prudent, Emma L. Baple

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

The authors apologize for errors in the labelling of p.(Asn547Lysfs∗42) and p.(Trp406Glyfs∗26) variants in Fig. 1A and D and Table 1. These have been corrected.

Original language	English
Pages (from-to)	E103
Journal	Brain
Volume	145
Issue number	10
DOIs	https://doi.org/10.1093/brain/awac254
Publication status	Published - Oct 1 2022

ASJC Scopus subject areas

Clinical Neurology

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Tábara, L. C., Al-Salmi, F., Maroofian, R., Al-Futaisi, A. M., Al-Murshedi, F., Kennedy, J., Day, J. O., Courtin, T., Al-Khayat, A., Galedari, H., Mazaheri, N., Protasoni, M., Johnson, M., Leslie, J. S., Salter, C. G., Rawlins, L. E., Fasham, J., Al-Maawali, A., Voutsina, N., ... Baple, E. L. (2022). Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123). Brain, 145(10), E103. https://doi.org/10.1093/brain/awac254

Tábara, LC, Al-Salmi, F, Maroofian, R, Al-Futaisi, AM, Al-Murshedi, F, Kennedy, J, Day, JO, Courtin, T, Al-Khayat, A, Galedari, H, Mazaheri, N, Protasoni, M, Johnson, M, Leslie, JS, Salter, CG, Rawlins, LE, Fasham, J, Al-Maawali, A, Voutsina, N, Charles, P, Harrold, L, Keren, B, Kunji, ERS, Vona, B, Jelodar, G, Sedaghat, A, Shariati, G, Houlden, H, Crosby, AH, Prudent, J & Baple, EL 2022, 'Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123)', Brain, vol. 145, no. 10, pp. E103. https://doi.org/10.1093/brain/awac254

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title = "Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123)",

abstract = "The authors apologize for errors in the labelling of p.(Asn547Lysfs∗42) and p.(Trp406Glyfs∗26) variants in Fig. 1A and D and Table 1. These have been corrected.",

author = "T{\'a}bara, {Luis Carlos} and Fatema Al-Salmi and Reza Maroofian and Al-Futaisi, {Amna Mohammed} and Fathiya Al-Murshedi and Joanna Kennedy and Day, {Jacob O.} and Thomas Courtin and Aisha Al-Khayat and Hamid Galedari and Neda Mazaheri and Margherita Protasoni and Mark Johnson and Leslie, {Joseph S.} and Salter, {Claire G.} and Rawlins, {Lettie E.} and James Fasham and Almundher Al-Maawali and Nikol Voutsina and Perrine Charles and Laura Harrold and Boris Keren and Kunji, {Edmund R.S.} and Barbara Vona and Gholamreza Jelodar and Alireza Sedaghat and Gholamreza Shariati and Henry Houlden and Crosby, {Andrew H.} and Julien Prudent and Baple, {Emma L.}",

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TY - JOUR

T1 - Correction

T2 - TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123)

AU - Tábara, Luis Carlos

AU - Al-Salmi, Fatema

AU - Maroofian, Reza

AU - Al-Futaisi, Amna Mohammed

AU - Al-Murshedi, Fathiya

AU - Kennedy, Joanna

AU - Day, Jacob O.

AU - Courtin, Thomas

AU - Al-Khayat, Aisha

AU - Galedari, Hamid

AU - Mazaheri, Neda

AU - Protasoni, Margherita

AU - Johnson, Mark

AU - Leslie, Joseph S.

AU - Salter, Claire G.

AU - Rawlins, Lettie E.

AU - Fasham, James

AU - Al-Maawali, Almundher

AU - Voutsina, Nikol

AU - Charles, Perrine

AU - Harrold, Laura

AU - Keren, Boris

AU - Kunji, Edmund R.S.

AU - Vona, Barbara

AU - Jelodar, Gholamreza

AU - Sedaghat, Alireza

AU - Shariati, Gholamreza

AU - Houlden, Henry

AU - Crosby, Andrew H.

AU - Prudent, Julien

AU - Baple, Emma L.

PY - 2022/10/1

Y1 - 2022/10/1

N2 - The authors apologize for errors in the labelling of p.(Asn547Lysfs∗42) and p.(Trp406Glyfs∗26) variants in Fig. 1A and D and Table 1. These have been corrected.

AB - The authors apologize for errors in the labelling of p.(Asn547Lysfs∗42) and p.(Trp406Glyfs∗26) variants in Fig. 1A and D and Table 1. These have been corrected.

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U2 - 10.1093/brain/awac254

DO - 10.1093/brain/awac254

M3 - Comment/debate

C2 - 36076346

AN - SCOPUS:85140417540

SN - 0006-8950

VL - 145

SP - E103

JO - Brain

JF - Brain

IS - 10

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Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123)

Abstract

ASJC Scopus subject areas

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