机译:BCAP31- BCAP31-相关的脑病和复杂的运动障碍模仿线粒体脑病
Division of Clinical and Metabolic Genetics Department of Pediatrics University of TorontoThe;
Division of Clinical and Metabolic Genetics Department of Pediatrics University of TorontoThe;
Division of Clinical and Metabolic Genetics Department of Pediatrics University of TorontoThe;
Division of Clinical and Metabolic Genetics Department of Pediatrics University of TorontoThe;
BCAP31; deafness; dystonia and cerebral hypomyelination syndrome sensorineural hearing loss; encephalopathy; mitochondrial encephalopathy; movement disorder;
机译:BCAP31- BCAP31-相关的脑病和复杂的运动障碍模仿线粒体脑病
机译:勘误:FBXL4突变导致线粒体脑病和线粒体DNA维持障碍(美国人类遗传学杂志(2013)93(471-481))
机译:FBXL4突变导致线粒体脑病和线粒体DNA维持障碍
机译:利用卷积神经网络对新生儿脑电图缺氧缺血性脑病的严重程度进行分级
机译:作为新生儿缺氧缺血性脑病的线粒体靶向治疗策略的光致态调节
机译:Glut1缺乏症作为脑病的原因包括认知残疾治疗婴儿癫痫和复杂的运动障碍
机译:线粒体半胱氨酰-tRNa合成酶基因CaRs2的突变导致严重的癫痫性脑病和复杂的运动障碍