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J Pediatr. 1999 Jun;134(6):777-9.

Prothrombin G20210A mutation in a child with spinal cord infarction.

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1
Departments of Hematology/Oncology and Neurology, Children's National Medical Center, George Washington University, Washington, DC., USA.

Abstract

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.

PMID:
10356151
[Indexed for MEDLINE]
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