Early-age Ndufs4 knockout mice are an inappropriate animal model of Leigh syndrome

被引:0
作者
Josef Finsterer
机构
[1] Krankenanstalt Rudolfstiftung,Neurology
[2] Messerli Institute,undefined
来源
Radiological Physics and Technology | 2019年 / 12卷
关键词
Metabolic myopathy; Brain; Leigh syndrome; Animal model; Mice; Knockout; Complex-I; Respiratory chain;
D O I
暂无
中图分类号
学科分类号
摘要
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页码:230 / 231
页数:1
相关论文
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Takahashi Y(2008)Leigh and Leigh-like syndrome in children and adults Pediatr Neurol 27 976-984
[3]  
Ohki A(2017)Diagnostic value of MRS-quantified brain tissue lactate level in identifying children with mitochondrial disorders Eur Radiol 173 596-600
[4]  
Shintani Y(2017)A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population Am J Med Genet A 6 19517-undefined
[5]  
Higuchi T(2016)Lactate chemical exchange saturation transfer (LATEST) imaging in vivo a biomarker for LDH activity Sci Rep undefined undefined-undefined
[6]  
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