Mitochondrial genetics: principles and practice.
作者信息
Shoffner J M, Wallace D C
出版信息
Am J Hum Genet. 1992 Dec;51(6):1179-86.
Abstract
摘要
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本文引用的文献
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Arch Neurol. 1983 Jan;40(1):2-6. doi: 10.1001/archneur.1983.04050010022005.
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Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature.伴有破碎红纤维（线粒体异常）的肌阵挛性癫痫：疾病实体还是综合征？两例病例的光镜和电镜研究及文献复习
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Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts.培养的人成纤维细胞中线粒体DNA多态性的母系遗传。
Somatic Cell Genet. 1981 Jan;7(1):103-8. doi: 10.1007/BF01544751.
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Maternal inheritance of human mitochondrial DNA.人类线粒体DNA的母系遗传
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Maternally inherited mitochondrial myopathy and myoclonic epilepsy.母系遗传的线粒体肌病和肌阵挛性癫痫。
Ann Neurol. 1985 Mar;17(3):228-37. doi: 10.1002/ana.410170303.
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Myoglobin expression: early induction and subsequent modulation of myoglobin and myoglobin mRNA during myogenesis.肌红蛋白表达：在肌生成过程中肌红蛋白和肌红蛋白mRNA的早期诱导及随后的调节。
Mol Cell Biol. 1986 Dec;6(12):4539-47. doi: 10.1128/mcb.6.12.4539-4547.1986.
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Thymine glycol lesions terminate chain elongation by DNA polymerase I in vitro.胸腺嘧啶乙二醇损伤在体外可终止DNA聚合酶I的链延伸。
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Normal oxidative damage to mitochondrial and nuclear DNA is extensive.线粒体和核DNA的正常氧化损伤广泛存在。
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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.与莱伯遗传性视神经病变相关的线粒体DNA突变。
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