Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlap

被引：3
|
作者：
Liu, Fuchen [1 ,2 ]
Zhang, Dong [1 ]
Yan, Chuanzhu [1 ,3 ,4 ]
机构：
[1] Shandong Univ, Qilu Hosp, Lab Neuromuscular Disorders, Dept Neurol, Jinan, Peoples R China
[2] Yale Univ, Kavli Inst Neurosci, Dept Neurobiol, New Haven, CT 06520 USA
[3] Shandong Univ, Sch Med, Minist Educ, Key Lab Expt Teratol, Jinan, Shandong, Peoples R China
[4] Brain Sci Res Inst, Jinan, Shandong, Peoples R China
来源：
NEUROLOGY INDIA | 2016年 / 64卷 / 02期
关键词：
D O I：
10.4103/0028-3886.177607
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
引用
收藏
页码：336 / U208
页数：3
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