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公开(公告)号:US20120276560A1
公开(公告)日:2012-11-01
申请号:US13329036
申请日:2011-12-16
IPC分类号: G01N33/566 , G01N33/577
CPC分类号: G01N33/6893 , G01N2333/70503 , G01N2440/38 , G01N2800/52
摘要: The present invention relates to methods of diagnosing, monitoring and assessing conditions of sialic acid deficiency such as Hereditary Inclusion Body Myopathy (HIBM) and to methods of predicting/determining responsiveness to treatment.
摘要翻译: 本发明涉及诊断,监测和评估诸如遗传性包涵体肌病(HIBM)的唾液酸缺乏症状的方法以及预测/确定对治疗反应性的方法。