ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder
Al-Hassnan, Z. N., Al-Dosary, M., Alfadhel, M., Faqeih, E. A., Alsagob, M., Kenana, R., Almass, R., Al-Harazi, O. S., Al-Hindi, H., Malibari, O. I., Almutari, F. B., Tulbah, S., Alhadeq, F., Al-SheddiVolume:
52
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2014-102592
Date:
March, 2015
File:
PDF, 5.47 MB
english, 2015