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Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration.

作者信息

Reichmann H, Rohkamm R, Zeviani M, Servidei S, Ricker K, DiMauro S

出版信息

Arch Neurol. 1986 Sep;43(9):957-61. doi: 10.1001/archneur.1986.00520090081024.

DOI:10.1001/archneur.1986.00520090081024
PMID:3741216
Abstract
摘要

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Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration.由于复合物III缺乏且可还原细胞色素b浓度正常导致的线粒体肌病。
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A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b.
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A new mitochondrial myopathy. Biochemical studies revealing a deficiency in the cytochrome b-c1 complex (complex III) of the respiratory chain.一种新的线粒体肌病。生化研究显示呼吸链的细胞色素b-c1复合物（复合物III）存在缺陷。
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Mitochondrial DNA mutations in multiple symmetric lipomatosis.多发性对称性脂肪瘤病中的线粒体DNA突变
Mol Cell Biochem. 1997 Sep;174(1-2):271-5.
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Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study.卡恩斯-塞尔综合征的肌病理学进展：一项形态学随访研究。
Acta Neuropathol. 1993;85(6):679-81. doi: 10.1007/BF00334681.
3
3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.一名患有卡恩斯-塞尔综合征患者的线粒体DNA发生3.1千碱基缺失。
Acta Neuropathol. 1995;90(2):126-9. doi: 10.1007/BF00294310.
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The biochemical basis of mitochondrial diseases.线粒体疾病的生化基础。
J Bioenerg Biomembr. 1988 Apr;20(2):161-91. doi: 10.1007/BF00768393.
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Variability in the activity of respiratory chain enzymes in mitochondrial myopathies.线粒体肌病中呼吸链酶活性的变异性。
Acta Neuropathol. 1988;76(2):135-41. doi: 10.1007/BF00688097.
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Defects in the cytochrome bc1 complex in mitochondrial diseases.
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Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity.
Eur J Pediatr. 1988 May;147(4):418-21. doi: 10.1007/BF00496424.
8
Mitochondrial myopathies.线粒体肌病
J Inherit Metab Dis. 1987;10 Suppl 1:113-28. doi: 10.1007/BF01812852.
9
Emetine-induced myopathy and carnitine deficiency.依米丁诱导的肌病和肉碱缺乏症。
J Neurol. 1990 Dec;237(8):495-6. doi: 10.1007/BF00314772.
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Myopathy in Williams-Beuren syndrome.威廉姆斯-贝伦综合征中的肌病
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