TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia
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Jacob O Day | R. Maroofian | H. Houlden | E. Baple | A. Crosby | J. Prudent | A. Sedaghat | A. Al-Maawali | G. Shariati | Lettie E Rawlins | Neda Mazaheri | B. Keren | P. Charles | Claire G. Salter | Nikol Voutsina | B. Vona | E. Kunji | F. al-Murshedi | C. Salter | T. Courtin | Gholamreza Jelodar | Joanna Kennedy | Mark Johnson | Aisha Al-Khayat | J. Fasham | Fatema Al-Salmi | Luis-Carlos Tábara | Amna Al-Futaisi | M. Protasoni | H. Galedari | Joseph S. Leslie | L. Harrold | Mark H. Johnson | F. Al-Murshedi | A. Al-Khayat | Fathiya Al-Murshedi
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