M. Alfadhel, M. Nashabat, M. T. Alrifai, H. Alshaalan, A. Mutairi et al., Further delineation of the phenotypic spectrum of ISCA2 defect: a report of ten new cases, Eur J Paediatr Neurol, vol.22, pp.46-55, 2018.

Z. N. Al-hassnan, A. , M. Alfadhel, M. Faqeih, E. A. Alsagob et al., ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder, J Med Genet, vol.52, pp.186-194, 2015.

J. Finsterer and M. Frank, Glucocorticoids for mitochondrial disorders, Singap Med J, vol.56, pp.122-123, 2015.

J. Finsterer and S. Zarrouk-mahjoub, Involvement of the spinal cord in mitochondrial disorders (MIDs), J Neurosci Rural Pract, vol.9, pp.245-251, 2018.

I. Toldo, M. Nosadini, C. Boscardin, G. Talenti, R. Manara et al., Neonatal mitochondrial leukoencephalopathy with brain and spinal involvement and high lactate: expanding the phenotype of ISCA2 gene mutations, Metab Brain Dis, vol.33, pp.805-812, 2018.