Heterozygous non-synonymous ROBO2 variants are unlikely to be sufficient to cause familial vesicoureteric reflux
Author:
Publisher
Elsevier BV
Subject
Nephrology
Reference27 articles.
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1. Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract;Kidney International;2022-05
2. Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms;Human Molecular Genetics;2022-03-26
3. Investigation of DNA variants specific to ROBO2 Isoform ‘a’ in Irish vesicoureteric reflux patients reveals marked CpG island variation;Scientific Reports;2020-02-10
4. Intrauterine low-protein diet aggravates developmental abnormalities of the urinary system via the Akt/Creb3 pathway in Robo2 mutant mice;American Journal of Physiology-Renal Physiology;2020-01-01
5. Disruption of Robo2-Baiap2 integrated signaling drives cystic disease;JCI Insight;2019-09-19
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