Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation

Chin Med J (Engl). 2019 Mar 20;132(6):716-718. doi: 10.1097/CM9.0000000000000139.

Authors

Xue-Bi Xu^{1

2}, Kun-Qian Ji^{1

2}, Jing-Wei Lyu^{1

2}, Shu Zhang¹, Xiao-Qing Lyu¹, Chang Liu¹, Wei Li¹, Chuan-Zhu Yan^{1

2

3}, Yu-Ying Zhao¹

Affiliations

¹ Research Institute of Neuromuscular and Neurodegenerative Diseases and Department of Neurology, Qilu Hospital, Shandong University, Jinan, Shandong 250000, China.
² Brain Science Research Institute, Shandong University, Jinan, Shandong 250000, China.
³ Mitochondrial Medicine Laboratory, Qilu Hospital, Shandong University, Qingdao, Shandong 266035, China.

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

DNA, Mitochondrial / genetics*
Humans
MELAS Syndrome / diagnosis*
MELAS Syndrome / diagnostic imaging
MELAS Syndrome / genetics*
Magnetic Resonance Imaging
Male
Middle Aged
Mutation / genetics

Substances

DNA, Mitochondrial