Applications of next-generation whole exome sequencing

被引:7
|
作者
Harding K.E. [1 ]
Robertson N.P. [1 ]
机构
[1] Department of Neurology, Institute of Psychological Medicine and Clinical Neuroscience, Cardiff University, Cardiff
基金
英国医学研究理事会;
关键词
Sanger Sequencing; Intellectual Disability; Exome Sequencing; Pathogenic Mutation; Validation Cohort;
D O I
10.1007/s00415-014-7372-1
中图分类号
学科分类号
摘要
[No abstract available]
引用
收藏
页码:1244 / 1246
页数:2
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