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[Fibrinogen gamma-chain mutation, p.Ile171His, leads to hereditary hypofibrinogenemia].

Zhonghua nei ke za zhi - 1 Feb 2022

Liu J X, Wang C J, Dai J H, Zhang M X, Lyu B, Jiang Bin

Abstract excerpt

Objective: To explore the clinical phenotype and genotype of a family with hereditary hypofibrinogenemia. Methods: Activated partial thrombin time (APTT), prothrombin time (PT),thrombin time (TT) and thrombelastogram (TEG) were tested in all family members. Fibrinogen activity and antigen were detected by Clauss method and immunoturbidimetric method respectively. All exons and flanking sequences of fibrinogen...

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PMID: 35090252
DOI: 10.3760/cma.j.cn112138-20210305-00182

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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