WHOLE-EXOME SEQUENCING AND RUNS OF HOMOZYGOSITY IDENTIFIES A NOVEL MUTATION OF DYX1C1 IN PRIMARY CILIARY DYSKINESIA FROM AN INBRED CHINESE FAMILY

被引:0
|
作者
Guo, Ting [1 ,2 ]
Luo, Hong [1 ,2 ]
机构
[1] Cent S Univ, Xiangya Hosp 2, Dept Resp Med, Changsha, Hunan, Peoples R China
[2] Cent S Univ, Res Unit Resp Dis, Changsha, Hunan, Peoples R China
关键词
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暂无
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
AP215
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页码:171 / 171
页数:1
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