학술논문
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
Document Type
Article
Author
Tábara, L.C.; Protasoni, M.; Johnson, M.; Kunji, E.R.S.; Prudent, J.; Al-Salmi, F.; Kennedy, J.; Day, J.O.; Leslie, J.S.; Salter, C.G.; Rawlins, L.E.; Fasham, J.; Voutsina, N.; Harrold, L.; Crosby, A.H.; Baple, E.L.; Maroofian, R.; Houlden, H.; Al-Futaisi, A.M.; Al-Murshedi, F.; Al-Maawali, A.; Courtin, T.; Charles, P.; Keren, B.; Al-Khayat, A.; Galedari, H.; Mazaheri, N.; Vona, B.; Jelodar, G.; Sedaghat, A.; Shariati, G.
Source
In: Brain . (Brain, 1 September 2022, 145(9):3095-3107)
Subject
Language
English
ISSN
14602156
00068950
00068950