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Article

Type I cystinuria and its genetic basis in a population of Turkish school children.

International journal of urology : official journal of the Japanese Urological Association - 1 Oct 2007

Tanzer Fatos, Ozgur Arzu, Bardakci Fevzi

Abstract excerpt

OBJECTIVES: Cystinuria is a common inherited disorder characterized by an abnormal urinary excretion of cystine and dibasic amino acids resulting in nephrolithiasis. The SLC3A1 gene, which encodes a dibasic amino acid transporter protein, is involved in the pathogenesis of cystinuria. In the present study we aimed to investigate the prevalence of cystinuria among children in Sivas province (Central Anatolia,...

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Identifiers

PMID: 17880288
DOI: 10.1111/j.1442-2042.2007.01852.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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