Treatment of myopathic form of coenzyme Q10 deficiency caused by electron-transferring-flavoprotein dehydrogenase (ETFDH) gene mutations

被引：0
|
作者：
Topaloglu, H. [1 ]
Gempel, K. [2 ,3 ,4 ]
Talim, B. [5 ]
Schneiderat, P. [6 ]
Schoser, B. [6 ]
Volkmar, H. [7 ]
Kale, G. [5 ]
Tokatli, A. [8 ]
Quinzii, C. [9 ]
Hirano, M. [9 ]
Naini, A. [9 ]
Di Mauro, S. [9 ]
Prokisch, H. [10 ]
Lochmueller, H. H. [6 ]
Horvath, R. [11 ]
机构：
[1] Hacettepe Univ, Dept Pediat, Child Neurol Unit, Ankara, Turkey
[2] Acad Hosp Schwabing, Metab Dis Ctr Munich Schwabing, Inst Clin Chem, Munich, Germany
[3] Acad Hosp Schwabing, Metab Dis Ctr Munich Schwabing, Inst Mol Diagnost, Munich, Germany
[4] Acad Hosp Schwabing, Metab Dis Ctr Munich Schwabing, Inst Mitochondrial Genet, Munich, Germany
[5] Hacettepe Univ, Dept Pediat, Pediat Pathol Unit, Ankara, Turkey
[6] Univ Munich, Friedrich Baur Inst, Dept Neurol, Munich, Germany
[7] Inst Neuropathol, Evangel Krankenhaus Bielefeld, Bielefeld, Germany
[8] Hacettepe Univ, Dept Pediat, Pediat Nutr & Metab Unit, Ankara, Turkey
[9] Columbia Univ, Med Ctr, Dept Neurol, New York, NY USA
[10] Tech Univ, GSF, Natl Res Ctr, Inst Human Genet, Munich, Germany
[11] Univ Munich, Ctr Med Genet, Friedrich Baur Inst, Dept Neurol, Munich, Germany
来源：
NEUROMUSCULAR DISORDERS | 2007年 / 17卷 / 9-10期
关键词：
D O I：
10.1016/j.nmd.2007.06.225
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：827 / 828
页数：2
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