A homozygous truncating ETV4 variant in a Nigerian family with congenital anomalies of the kidney and urinary tract is a research paper published in American Journal of Medical Genetics Part A (2023). On theSindex it has a DataRank of 0. It has been cited 3 times.
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Deutsche Forschungsgemeinschaft
Grant: KO6579/2‐1 (708037–809683)
Deutsche Forschungsgemeinschaft
Grant: 499462148
Deutsche Forschungsgemeinschaft
Grant: ME5722/1‐1 (707802–809379)
Deutsche Forschungsgemeinschaft
Grant: 442070894
National Institutes of Health
Grant: 5T32DK007726‐37
National Institutes of Health
Grant: DK076683
National Institutes of Health
Grant: DK068306
NIDDK NIH HHS
Grant: R01 DK068306
NIDDK NIH HHS
Grant: R01 DK076683
NIDDK NIH HHS
Grant: T32 DK007726
NHGRI NIH HHS
Grant: U54 HG006504
National Institutes of Health
Grant: 5R01DK076683-08
Discover and functionally characterize full-penetrance causes of nephrosis/FSGS
National Institutes of Health
Grant: 5T32DK007726-37
Research Training in Pediatric Nephrology
National Institutes of Health
Grant: 1U54HG006504-01
Yale Center for Mendelian Disorders
National Institutes of Health
Grant: 5R01DK068306-17
Novel genetics, pathobiology and therapy of nephronophthisis-related ciliopathies
Deutsche Forschungsgemeinschaft
Grant: unidentified
unidentified
FWCI
0.28
Citation Percentile
0.5%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals