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Article

[Pedigree survey in a family with hereditary protein S deficiency].

Zhonghua xin xue guan bing za zhi - 24 Sept 2016

Huang K Y, Kong L Q, Wu Z, Wen X, Zhao J, Zhang H C, Xu Y, Long X J, Kang Y

Abstract excerpt

Objective: To observe the clinical feature of familiar hereditary protein S deficiency(HPSD), and to explore the related gene mutations. Methods: A total of seven family members were enrolled in this study and examined during the June to September 2015. Medical histories of the families were analyzed to detect HPSD according to the diagnostic criteria. PROS1 genes of the proband and her family were analyzed. DNA...

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Source

Identifiers

PMID: 27667277
DOI: 10.3760/cma.j.issn.0253-3758.2016.09.010

Genes

PROS1

Variants

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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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