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

QJM. 2024 Feb 26:hcae036. doi: 10.1093/qjmed/hcae036. Online ahead of print.

Authors

Feifei Xie¹, Lin Zhou¹, Peng Luo², Hui Xi¹, Wenxian Yu¹, Na Ma¹, Dan Wang¹, Ying Peng¹

Affiliations

¹ National Health Commission Key Laboratory of Birth Defects for Research and Prevention, Hunan Provincial Maternal and Child Health Care Hospital, Changsha, Hunan, 410008, China.
² Yongzhou Maternal and Child Health Care Hospital, Yongzhou, Hunan, 425199, China.

PMID: 38410081
DOI: 10.1093/qjmed/hcae036

No abstract available