目的探讨肌阵挛癫痫伴破碎红纤维综合征（MERRF）的分子遗传学特点。
Objective To study the characteristics of molecular genetics concerning Chinese myoclonic epilepsy and ragged-red fiber disease (MERRF).
骨骼肌活检病理检查可见破碎样红纤维及异常线粒体。
The biopsy in the skeletal muscle showed ragged red fiber and abnormal mitochondria.
骨骼肌活检病理检查可见破碎样红纤维及异常线粒体。
The biopsy in the skeletal muscle showed ragged red fiber and abnormal mitochondria.
应用推荐