A NEW GENETIC CAUSE OF PRIMARY COENZYME Q10 DEFICIENCY

被引：0
|
作者：
Rahman, S. [1 ,2 ]
Duncan, A. J. [1 ]
Bitner-Glindziez, M. [1 ]
Meunier, B. [3 ]
Costello, H. [1 ]
Hargreaves, I. P. [4 ]
Lopez, L. C. [5 ]
Hirano, M. [5 ]
Quinzii, C. M. [5 ]
Sadowski, M. I. [6 ]
Singleton, A. [7 ]
Clayton, P. T. [1 ]
机构：
[1] UCL Inst Child Hlth, Clin & Mol Genet Unit, London, England
[2] Natl Hosp Neurol & Neurosurg, MRC, Neuromuscular Res Ctr, London WC1N 3BG, England
[3] CNRS, Ctr Genet Mol, Gif Sur Yvette, France
[4] Natl Hosp Neurol & Neurosurg, Neurometab Unit, London WC1N 3BG, England
[5] Columbia Univ, Med Ctr, New York, NY USA
[6] Natl Inst Med Res, Div Math Biol, London NW7 1AA, England
[7] NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
来源：
MOLECULAR GENETICS AND METABOLISM | 2009年 / 98卷 / 1-2期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
113
引用
收藏
页码：5 / 5
页数：1
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