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Article

Methylenetetrahydrofolate reductase polymorphism in childhood primary focal segmental glomerulosclerosis.

Nephron - 1 Oct 2002

Zou Chaochun, Tsukahara Hirokazu, Hiraoka Masahiro, Mizu Jiang, Todoroki Yukiko, Ohshima Yusei, Kimura Hideki, Tsuzuki Kazuo, Mayumi Mitsufumi

Abstract excerpt

AIM: The purpose of this study was to evaluate the association between the methylenetetrahydrofolate reductase (MTHFR) C/T polymorphism and the prevalence and course of focal segmental glomerulosclerosis (FSGS) in our pediatric population. METHODS: Genotypes for MTHFR were determined in 15 primary FSGS patients (male/female, 6/9) and 238 control subjects (male/female, 110/128) by the polymerase chain reaction and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glomerulosclerosis, Focal Segmental

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Share to Kidney Failure, Chronic

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Oxidoreductases Acting on CH-NH Group Donors

Share to Polymorphism, Restriction Fragment Length

Source

Identifiers

PMID: 12218328
DOI: 10.1159/000063283

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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