TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
Luis Carlos Tábara(University of Cambridge), Emma L. Baple(University of Exeter), Boris Keren(Sorbonne Université), Joanna Kennedy(University of Exeter), Fatema Al-Salmi(Sultan Qaboos University), Gholamreza Jelodar(Ahvaz Jundishapur University of Medical Sciences), Hamid Galedari(Shahid Chamran University of Ahvaz), Almundher Al‐Maawali(Sultan Qaboos University Hospital), Nikol Voutsina(University of Exeter), Margherita Protasoni(Granta Design (United Kingdom)), Barbara Vona(Brigham and Women's Hospital), Alireza Sedaghat(Ahvaz Jundishapur University of Medical Sciences), Thomas Courtin(Sorbonne Université), James Fasham(University of Exeter), Julien Prudent(University of Cambridge), Edmund R.S. Kunji(University of Cambridge), Neda Mazaheri(Shahid Chamran University of Ahvaz), Joseph S. Leslie(University of Exeter), Lettie E. Rawlins(Royal Devon and Exeter Hospital), Claire Salter(Birmingham Women’s and Children’s NHS Foundation Trust), Henry Houlden(Queen Mary University of London), Laura Harrold(University of Exeter), Reza Maroofian(University College London), Perrine Charles(School of the Art Institute of Chicago), Gholamreza Shariati(Ahvaz Jundishapur University of Medical Sciences), Amna Al‐Futaisi(Sultan Qaboos University Hospital), Jacob Day(University of Exeter), Mark Johnson(University of Cambridge), Andrew H Crosby(Royal Devon and Exeter Hospital), Fathiya Al-Murshedi(Sultan Qaboos University), Aisha Al‐Khayat(Sultan Qaboos University)
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