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Article

Genetic screening of candidate genes for a prothrombotic interaction with type I protein C deficiency in a large kindred.

Thrombosis and haemostasis - 1 Jan 2001

Scott B T, Bovill E G, Callas P W, Hasstedt S J, Leppert M F, Valliere J E, Varvil T S, Long G L

Abstract excerpt

The incomplete penetrance of thrombosis in familial protein C deficiency suggests disease occurs when this deficit is combined with additional abnormalities in the hemostatic system. The pattern of inherited thrombophilia in the Vermont II kindred, which is affected by a clinically dominant type I protein C deficiency, provides strong evidence for a second unidentified gene that segregates independently of...

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PMID: 11204593

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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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