Acylcarnitine profile mimicking multiple acyl-CoA dehydrogenase deficiency in a patient with mitochondrial myopathy and a mutation in MT-CO2

被引：0
|
作者：
Roos, S. [1 ]
Sofou, K. [2 ]
Hedberg-Oldfors, C. [1 ]
Kollberg, G. [1 ]
Lindgren, U. [1 ]
Thomsen, C. [1 ]
Asin-Cayuela, J. [1 ]
Tulinius, M. [2 ]
Oldfors, A. [1 ]
机构：
[1] Univ Gothenburg, Inst Biomed, Gothenburg, Sweden
[2] Sahlgrens Univ Hosp, Queen Silvia Childrens Hosp, Gothenburg, Sweden
来源：
NEUROMUSCULAR DISORDERS | 2017年 / 27卷
关键词：
D O I：
10.1016/j.nmd.2017.06.096
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P.66
引用
收藏
页码：S118 / S118
页数：1
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