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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 pres...

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Identifiers

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

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17880288-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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