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Article

The novel and independent association between single-point SNP of NPHP4 gene and renal function in non-diabetic Japanese population: the Takahata study.

Journal of human genetics - 1 Dec 2010

Konta Tsuneo, Takasaki Satoshi, Ichikawa Kazunobu, Emi Mitsuru, Toriyama Sayumi, Satoh Hitoshi, Ikeda Ami, Suzuki Kazuko, Mashima Yusuke, Shibata Yoko, Watanabe Tetsu, Kato Takeo, Kawata Sumio, Kubota Isao

Abstract excerpt

Nephronophthisis (NPHP) 4 gene coding nephrocystin-4 is involved in the development of renal tubules and its congenital mutations cause juvenile end-stage renal disease, NPHP. To investigate the association between single-point single-nucleotide polymorphism (SNP) of NPHP4 gene and renal function...

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Identifiers

PMID: 20844548
DOI: 10.1038/jhg.2010.113

Genes

NPHP4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20844548-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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