Brain atrophy in a patient with mitochondrial DNA G8363A mutation  

作　　者：Hong-Liang Xu Ya-Jun Lian Xin Chen 

机构地区：[1]Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China

出　　处：《Chinese Medical Journal》2019年第17期2141-2142,共2页中华医学杂志（英文版）

摘　　要：To the Editor: Mitochondrial diseases are a common group of human genetic diseases that can occur at any decade of life. Mitochondrial DNA (mtDNA) mutations are responsible for most adult-onset mitochondrial diseases.[1] There are over 260 known pathogenic mutations in mtDNA.[2] In the last two decades, a large number of pathogenic mutations of mtDNA have been reported, which associate with a wide spectrum of clinical features.[3]

关 键 词：There ARE In the LAST a large NUMBER of 

分 类 号：R[医药卫生]