Whole exome sequencing reveals two novel mutations in GREB1L in two chinese families with renal agenesis

被引:1
|
作者
Xie, Feifei [1 ]
Zhou, Lin [1 ]
Luo, Peng [2 ]
Xi, Hui [1 ]
Yu, Wenxian [1 ]
Ma, Na [1 ]
Wang, Dan [1 ,3 ]
Peng, Ying [1 ,3 ]
机构
[1] Hunan Prov Maternal & Child Hlth Care Hosp, Key Lab Birth Defects Res & Prevent, Natl Hlth Commiss, Changsha 410008, Hunan, Peoples R China
[2] Yongzhou Maternal & Child Hlth Care Hosp, Yongzhou 425199, Hunan, Peoples R China
[3] Hunan Prov Maternal & Child Hlth Care Hosp, Prenatal Diag Ctr, Key Lab Birth Defects Res & Prevent, Natl Hlth Commiss, Changsha 410008, Hunan, Peoples R China
关键词
D O I
10.1093/qjmed/hcae036
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:462 / 464
页数:3
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