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[Analysis of the gene mutation in an inherited FVII deficiency patient].

Zhonghua yi xue za zhi - 12 May 2015

Li Ruibing, Zhang Manli, Wang Zhengguan, Liu Ping, Duan Jinyan, Wang Chengbin, Lu Yanping

Abstract excerpt

OBJECTIVE: The identify the gene defect of an inherited FVII deficiency patient. METHODS: The promoter, all the exons and exon-intron boundaries and 3' UTR of F7 gene of the proband were analyzed by direct sequencing. The defected mutations were confirmed by sequencing the complementary strand. The mutations would be screened in the related database and 150 healthy donors to identify the SNP. By splice site...

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PMID: 26178358

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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