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[Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 1 Sept 2004

Wang Wen-bin, Wang Hong-li, Wang Xue-feng, Fu Qi-hua, Zhou Rong-fu, Xie Shuang, Hu Yi-qun, Wang Zhen-yi

Abstract excerpt

OBJECTIVE: To explore the molecular mechanisms involved in a pedigree with inherited coagulation factor X (FX) deficiency. METHODS: The activated partial thromboplastin time (APTT), prothrombin time (PT), FX activity (FX:C) and FX antigen (FX:Ag) test were adopted for phenotype diagnosis. All the 8 exons, intron/exon boundaries and the 5'untranslated regions (UTR) of the FX gene were amplified by polymerase chain...

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PMID: 15569527

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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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