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

来源：

QJM-AN INTERNATIONAL JOURNAL OF MEDICINE | 2024年 / 117卷 / 06期

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

页码：462 / 464

页数：3

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