ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder
暂无分享,去创建一个
Olfat Al-Harazi | N. Kaya | D. Çolak | E. Faqeih | F. Al-Mohanna | M. Alfadhel | Z. Al-Hassnan | H. Al-Hindi | Makki A Almuntashri | R. Kenana | A. Alasmari | T. Al-Sheddi | S. Tulbah | M. Alsagob | R. Almass | M. Al-Dosary | Omhani I Malibari | Faten B Almutari | Faten Alhadeq | Rana Alamro | H. Alshaalan | T. Al‐Sheddi | Rawan Almass | Tarfa Al‐Sheddi | Makki Almuntashri