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

页码：5 / 5

页数：1

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