ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder von Al-Hassnan, Zuhair N, Al-Dosary, Mazhor, Alfadhel, Majid, Faqeih, Eissa A, Alsagob, Maysoon, Kenana, Rosan, Almass, Rawan, Al-Harazi, Olfat S, Al-Hindi, Hindi, Malibari, Omhani I, Almutari, Faten B, Tulbah, Sahar, Alhadeq, Faten, Al-Sheddi, Tarfa, Alamro, Rana, AlAsmari, Ali, Almuntashri, Makki, Alshaalan, Hesham, Al-Mohanna, Futwan A, Colak, Dilek, Kaya, Namik

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