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Article

MTHFR homozygous mutation and additional risk factors for cerebral infarction in a large Italian family.

Pediatric neurology - 1 Jan 2009

Del Balzo Francesca, Spalice Alberto, Perla Massimo, Properzi Enrico, Iannetti Paola

Abstract excerpt

Several cases with cerebral infarctions associated with the C677T mutation in the methylenetetrahydrofolate reductase gene (MTHFR) have been reported. Given the large number of asymptomatic individuals with the MTHFR mutation, additional risk factors for cerebral infarction should be considered....

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Source

Identifiers

PMID: 19068258
DOI: 10.1016/j.pediatrneurol.2008.09.023

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19068258-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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