Blumenthal D T, Shanske S, Schochet S S, Santorelli F M, DiMauro S, Jaynesm M, Bodensteiner J
Department of Neurology, West Virginia University Hospitals, Morgantown, USA.
Neurology. 1998 Feb;50(2):524-5. doi: 10.1212/wnl.50.2.524.
In a patient with clinical features of myoclonus epilepsy with ragged red fibers (MERRF), molecular genetic analysis of mitochondrial DNA did not show either of the two point mutations typically associated with MERRF but did show multiple deletions by Southern blot. This case further illustrates the heterogeneity observed with mtDNA mutations.
在一名具有肌阵挛性癫痫伴破碎红纤维(MERRF)临床特征的患者中,线粒体DNA的分子遗传学分析未显示出通常与MERRF相关的两种点突变中的任何一种,但Southern印迹显示存在多个缺失。该病例进一步说明了线粒体DNA突变所观察到的异质性。