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Article

Rare STAT3 haplotypes cause a predisposition to developing congenital anomalies of the kidney and urinary tract disorder.

Turkish journal of medical sciences - 1 Jan 2024

Polat Mert, Şahin Feride İffet, Baskin Esra, Toprak Uğur, Gülleroğlu Kaan Savaş, Haberal Mehmet, Terzi Yunus Kasım

Abstract excerpt

Background/aim: Congenital anomalies of the kidney and urinary tract (CAKUT) are characterized by renal developmental disorders in the embryonic period. STAT3 is a member of the STAT protein family. The members of this protein family play roles in various cellular mechanisms, such as the early stages of embryonic development, kidney development, and renal diseases. This study aims to determine the frequency of...

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Identifiers

PMID: 39734345
DOI: 10.55730/1300-0144.5911
PMCID: PMC11673622

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