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Article

Congenital plasminogen deficiency caused by a Ser572 to Pro mutation.

Blood - 15 Jul 1993

Azuma H, Uno Y, Shigekiyo T, Saito S

Abstract excerpt

We used a polymerase chain reaction (PCR) strategy and restriction fragment polymorphism analysis to evaluate all 19 exons of the plasminogen (PLG) gene in a Japanese patient with congenital PLG deficiency and her family members. She presented with cerebral infarction. Sequence analysis following amplification of each exon and its flanking regions showed a single T to C transition in exon 14, which changed a...

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Identifiers

PMID: 8392398

Genes

PLG

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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