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Article

Prospective analysis of factor XI deficiencies in the Marseilles area identified four novel mutations among 12 consecutive unrelated families.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Jan 2009

Quélin Florence, Frère Corinne, Pouymayou Catherine, Morange Pierre, de Mazancourt Philippe, Juhan-Vague Irène

Abstract excerpt

Hereditary factor XI (FXI) deficiency is an autosomal bleeding disorder of variable severity but without a clear relationship between bleeding and FXI levels or mutation location or both. In the present study, the molecular basis of FXI deficiency in 16 patients from 12 families originating from...

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PMID: 20523169
DOI: 10.1097/MBC.0b013e32831bc51c

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20523169-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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