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[Identification of genetic defects in a Chinese pedigree with factor XIII deficiency: case report and literature review].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 1 Oct 2015

Xu Guanqun, Liang Qian, Zhang Liwei, Shen Yun, Ding Qiulan, Wang Xuefeng, Wang Hongli

Abstract excerpt

OBJECTIVE: To perform phenotypic diagnosis, genetic diagnosis and prenatal diagnosis of inherited coagulation factor XIII (FXIII)deficiency in a Chinese family also provide a review of inherited coagulation F XIII deficiency. METHODS: The activity levels of F XIII (F XIII:C) of proband and family members were measured by clot solubility test and REA-chrom F XIII kit. The antigen levels of F XIII(FXIII:Ag) were...

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PMID: 26477763
DOI: 10.3760/cma.j.issn.0253-2727.2015.10.008
PMCID: PMC7364940

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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