APA

Musa S., Eyaid W., Kamer K., Ali R., Al-Mureikhi M., Shahbeck N., Al Mesaifri F., Makhseed N., Mohamed Z., AlShehhi W. A., Mootha V. K., Juusola J. & Ben-Omran T. (2019). A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. : JIMD reports.

Chicago

Musa Sara, Eyaid Wafaa, Kamer Kimberli, Ali Rehab, Al-Mureikhi Mariam, Shahbeck Noora, Al Mesaifri Fatma, Makhseed Nawal, Mohamed Zakkiriah, AlShehhi Wafaa Ali, Mootha Vamsi K, Juusola Jane and Ben-Omran Tawfeg. 2019. A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. : JIMD reports.

Harvard

Musa S., Eyaid W., Kamer K., Ali R., Al-Mureikhi M., Shahbeck N., Al Mesaifri F., Makhseed N., Mohamed Z., AlShehhi W. A., Mootha V. K., Juusola J. and Ben-Omran T. (2019). A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. : JIMD reports.

MLA

Musa Sara, Eyaid Wafaa, Kamer Kimberli, Ali Rehab, Al-Mureikhi Mariam, Shahbeck Noora, Al Mesaifri Fatma, Makhseed Nawal, Mohamed Zakkiriah, AlShehhi Wafaa Ali, Mootha Vamsi K, Juusola Jane and Ben-Omran Tawfeg. A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients. : JIMD reports. 2019.