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Article

No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia.

Journal of medical genetics - 1 Nov 2004

Karabegovic A, Shinawi M, Cymerman U, Letarte M

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Share to Receptors, Cell Surface

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Identifiers

PMID: 15520401
DOI: 10.1136/jmg.2004.022079
PMCID: PMC1735618

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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No live individual homozygous for a novel endoglin mutation was found in a consanguineous Arab family with hereditary haemorrhagic telangiectasia.PMID 15520401Read ↗

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