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[Molecular mechanism analysis of a family with hereditary coagulation F Ⅺ deficiency caused by compound heterozygous mutations].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 14 Mar 2024

Chen Y, Qin L Y, Lin S R, Yang L L, Zhang K, Ye L Y, Jin Y H, Wang M S

Abstract excerpt

A 34 year old female patient was scheduled to undergo surgical resection due to a "breast nodule". Preoperative examination revealed an activated partial thromboplastin time (APTT) of 66.2 seconds, coagulation factor Ⅺ activity (FⅪ: C) of 2%, and FⅪ antigen (FⅪ: Ag) of 40.3%. The patient and family members showed no abnormal bleeding symptoms. Diagnosed as hereditary coagulation factor Ⅺ deficiency. Genetic...

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Identifiers

PMID: 38716603
DOI: 10.3760/cma.j.cn121090-20230814-00065
PMCID: PMC11078654

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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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