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Article

Prothrombin G20210A mutation in a child with spinal cord infarction.

The Journal of pediatrics - 1 Jun 1999

Young G, Krohn K A, Packer R J

Abstract excerpt

Prothrombin G20210A is a newly described common mutation that is associated with an increased risk of arterial and venous thrombosis. We describe a healthy child heterozygous for this prothrombin mutation who had a spinal cord infarct with no other prothrombotic risk factors.

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Source

Identifiers

PMID: 10356151
DOI: 10.1016/s0022-3476(99)70298-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10356151-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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