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

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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)

Brain

DOI: 10.1093/brain/awac254

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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.

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Tábara, L. C., Al-Salmi, F., Maroofian, R., Al-Futaisi, A. M., Al-Murshedi, F., Kennedy, J., … Baple, E. L. (2022, October 1). Correction: TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia (Brain (2022) 145:9 (3095-3107) DOI: 10.1093/brain/awac123). Brain. Oxford University Press. https://doi.org/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)

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