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Article

Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.

British journal of haematology - 1 Dec 1997

Wistinghausen B, Reischer A, Oddoux C, Ostrer H, Nardi M, Karpatkin M

Abstract excerpt

We investigated an 8-year-old Arab girl with severe factor XI deficiency; one sibling and her father also have severe factor XI deficiency. Her parents and her father's parents are first cousins. Restriction analysis and DNA sequencing excluded the type I, II, III and IV mutations. We demonstrate...

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Identifiers

PMID: 9401068
DOI: 10.1046/j.1365-2141.1997.4343244.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-9401068-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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