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散发性线粒体肌病中肌肉线粒体DNA的父系遗传缺失。

Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.

作者信息

Filosto Massimiliano, Mancuso Michelangelo, Vives-Bauza Cristofol, Vilà Maya R, Shanske Sara, Hirano Michio, Andreu Antoni L, DiMauro Salvatore

机构信息

Department of Neurology, Columbia University College of Physicians and Surgeons, New York, NY, USA.

出版信息

Ann Neurol. 2003 Oct;54(4):524-6. doi: 10.1002/ana.10709.

Abstract

In 2002, paternal inheritance of muscle mitochondrial DNA (mtDNA) was reported in a patient with exercise intolerance and a mitochondrial DNA (mtDNA) mutation restricted to skeletal muscle. To evaluate whether paternal inheritance is a common phenomenon, we studied 10 sporadic patients with skeletal muscle-restricted mtDNA mutations: five harbored mtDNA point mutations in protein-coding genes and five had single mtDNA deletions. We performed haplotype analysis and direct sequencing of the hypervariable regions 1 and 2 of the D-loop in muscle and blood from the patients and, when available, in blood from their parents. We did not observe paternal inheritance in any of our patients.

摘要

2002年,有报道称一名患有运动不耐受且线粒体DNA(mtDNA)突变局限于骨骼肌的患者存在肌肉线粒体DNA的父系遗传。为了评估父系遗传是否为常见现象,我们研究了10例散发的骨骼肌局限性mtDNA突变患者:其中5例在蛋白质编码基因中存在mtDNA点突变,5例存在单个mtDNA缺失。我们对患者肌肉和血液以及(若有)其父母血液中D环高变区1和2进行了单倍型分析和直接测序。我们在任何患者中均未观察到父系遗传现象。

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