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 journalComment/debatepeer-review


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 languageEnglish
Pages (from-to)E103
Issue number10
Publication statusPublished - Oct 1 2022

ASJC Scopus subject areas

  • Clinical Neurology

Cite this