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Article

Genotype-Phenotype Correlation of Hereditary Plasminogen Deficiency: Molecular Mechanisms From 18 Patients With Cerebral Infarction.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Jan 2026

Lu Yifan, Xie Haixiao, Yu Dandan, Jin Yanhui, Xu Fei, Wang Mingshan, Yang Lihong

Abstract excerpt

INTRODUCTION: Hereditary plasminogen (PLG) deficiency is a rare congenital fibrinolytic disorder and a rare disease. This study conducted gene sequencing and statistical analysis on patients with cerebral infarction (CI) and decreased PLG activity (PLG:A) to explore the relationship between PLG gene variants and hereditary thrombotic diseases. AIM: To analyse PLG gene variants in 18 patients with hereditary PLG...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 41778291
DOI: 10.1111/hae.70248

Genes

PLG

Variants

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