학술논문
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TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Academic Journal
Tábara, Luis Carlos; Al-Salmi, Fatema; Maroofian, Reza; Al-Futaisi, Amna Mohammed; 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, Almundher; Voutsina, Nikol; Charles, Perrine
Academic Journal
Al-Futaisi, Amna Mohammed; Al-Kindi, Mohammed Nasser; Al-Mawali, Al-Mundher; Koul, Roshan Lal; Al-Adawi, Samir; Al-Yahyaee, Said Ali
Academic Journal
Al-Futaisi, Amna Mohammed; Al-Kindi, Mohammed Nasser; Al-Maawali, Almundher; Koul, Roshan Lal; Al-Adawi, Samir; Al-Yahyaee, Said Ali
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[AR] Al-Futaisi, Amna Mohammed
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