Interleukin‐10‐1082A/G polymorphism is associated with renal parenchymal damage in congenital anomalies of the kidney and urinary tract
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DOI: 10.1111/nep.13229
Abstract: The aim of the study was to investigate whether the functional IL10‐1082A/G polymorphism exert a role in congenital anomalies of the kidney and urinary tract (CAKUT) in children. Also, the serum IL‐10 and its association… read more here.
Keywords: congenital anomalies; urinary tract; 1082a polymorphism; renal parenchymal ... See more keywords