Whole-exome sequencing identifiesFOXL2,FOXA2andFOXA3as candidate genes for monogenic congenital anomalies of the kidneys and urinary tract is a research paper published in Nephrology Dialysis Transplantation (2021). On theSindex it has a DataRank of 0. It has been cited 11 times.
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NIH
Grant: DK076683
NIH
Grant: DK088767
NIDDK NIH HHS
Grant: T32 DK007726
NHGRI NIH HHS
Grant: U54 HG006504
NCATS NIH HHS
Grant: UL1 TR001863
NIDDK NIH HHS
Grant: R01 DK088767
NIDDK NIH HHS
Grant: R01 DK076683
FWCI
0.37
Citation Percentile
0.6%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals