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Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations

Xiao-Lin Yu Chuan-Zhu Yan Kun-Qian Ji Peng-Fei Lin Xue-Bi Xu Ting-Jun Dai Wei Li Yu-Ying Zhao

中华医学杂志（英文版）2018，Vol.131Issue(22)：2705-2712,8.

中华医学杂志（英文版）2018，Vol.131Issue(22)：2705-2712,8.DOI:10.4103/0366-6999.245265

Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations

Xiao-Lin Yu ¹Chuan-Zhu Yan ²Kun-Qian Ji ³Peng-Fei Lin ²Xue-Bi Xu ⁴Ting-Jun Dai ⁵Wei Li ²Yu-Ying Zhao²

作者信息

1. Department of Geriatrics Medicine, Qilu Hospital, Shandong University, Jinan, Shandong 250012, China
2. Department of Neurology, Research Institute of Neuromuscular and Neurodegenerative Diseases, Qilu Hospital, Shandong University, Jinan, Shandong 250012, China
3. Key Laboratory of Cardiovascular Proteomics of Shandong Province, Qilu Hospital, Shandong University, Jinan, Shandong 250012, China
4. Mitochondrial Medicine Laboratory, Qilu Hospital(Qingdao), Shandong University, Qingdao, Shandong 266035, China
5. Brain Science Research Institute, Shandong University, Jinan, Shandong 250012, China
折叠

摘要

关键词

Clinical Features/Leigh Syndrome/Mitochondrial DNA/Neuroimaging/Pathology

Key words

Clinical Features/Leigh Syndrome/Mitochondrial DNA/Neuroimaging/Pathology

引用本文复制引用

Xiao-Lin Yu,Chuan-Zhu Yan,Kun-Qian Ji,Peng-Fei Lin,Xue-Bi Xu,Ting-Jun Dai,Wei Li,Yu-Ying Zhao..Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations[J].中华医学杂志（英文版）,2018,131(22):2705-2712,8.

基金项目

This study was supported by the grants from the National Natural Science Foundation of China (No.81671235 and 81701237) and the Taishan Scholars Program of Shandong Province. （No.81671235 and 81701237）

中华医学杂志（英文版）

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ISSN：0366-6999

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