Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families is a research paper published in Pediatric Nephrology (2023). On theSindex it has a DataRank of 0. It has been cited 5 times.
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National Institutes of Health
Grant: 5RC-2DK122397-02
NIH HHS
Grant: T5T32-DK007726-37
NIH HHS
Grant: 5R01-DK076683-16
U.S. Department of Defense
Grant: PR212415
NIDDK NIH HHS
Grant: R01 DK076683
U.S. Department of Defense
Grant: PR190746
NIDDK NIH HHS
Grant: RC2 DK122397
NIDDK NIH HHS
Grant: T32 DK007726
National Institutes of Health
Grant: 5R01DK076683-08
Discover and functionally characterize full-penetrance causes of nephrosis/FSGS
National Institutes of Health
Grant: 3RC2DK122397-04S1
Integrating large scale genomics and functional studies to accelerate FSGS/NS discovery
National Institutes of Health
Grant: 5T32DK007726-27
Research Training in Pediatric Nephrology
FWCI
0.74
Citation Percentile
0.7%
Citation Trend
Fields of Study
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Sustainable Development Goals