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线粒体心肌病:分子与生化分析

Mitochondrial cardiomyopathy: molecular and biochemical analysis.

作者信息

Marin-Garcia J, Goldenthal M J

机构信息

The Molecular Cardiology Institute, Highland Park, NJ 08904, USA.

出版信息

Pediatr Cardiol. 1997 Jul-Aug;18(4):251-60. doi: 10.1007/s002469900169.

Abstract

Abnormalities in cardiac mitochondrial respiratory enzymes and mitochondrial DNA have been found in an increasing number of pediatric cases of both dilated and hypertrophic cardiomyopathy, giving rise to the entity known as mitochondrial cardiomyopathy. Histochemical, biochemical, and molecular findings are described in this review of mitochondrial cardiomyopathy, which should provide assistance in its diagnostic identification.

摘要

在越来越多的扩张型和肥厚型心肌病儿科病例中,已发现心脏线粒体呼吸酶和线粒体DNA异常,从而产生了所谓的线粒体心肌病这一实体。本文对线粒体心肌病的综述描述了组织化学、生物化学和分子学研究结果,这应有助于其诊断识别。

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