多发性线粒体功能障碍综合征6 型1 例报告并文献复习

武宇辉, 张涛, 杨燕澜 - 临床儿科杂志, 2020 - jcp.xinhuamed.com.cn
ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder [J]. J Med Genet,
… variant responsible for an early-onset neurodegenerative mitochondrial disorder: a case …