Novel LRPPRC Mutation in a Boy With Mild Leigh Syndrome, French–Canadian Type Outside of Québec:

Child Neurology Open

Velda Xinying Han¹ 

关键词: children;    developmental delay;    epilepsy;    metabolism;    mitochondrial disorder;    neurodevelopment;   

DOI  :  10.1177/2329048X17737638

学科分类：儿科学

来源: Sage Journals

【 授权许可】

CC BY-NC