TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

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

TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia

Autor(en):

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

Tübinger Autor(en):

Vona, Barbara

Erschienen in:

Brain (2022), Bd. 145, H. 9, S. 3095-3107

Verlagsangabe:

Oxford : Oxford Univ. Press

Sprache:

Englisch

Referenz zum Volltext:

https://dx.doi.org/10.1093/brain/awac254

ISSN:

0006-8950