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Is hereditary haemorrhagic telangiectasia rare in the black race? The first sub-Saharan mutation.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Jan 2011

Westermann C J J, Kitonyi G W, Letteboer T G W

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Share to Activin Receptors, Type II
Share to Africa South of the Sahara
Share to Black People
Share to DNA Mutational Analysis

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

Share to Genetic Predisposition to Disease

Share to Mutation, Missense

Share to Telangiectasia, Hereditary Hemorrhagic

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Identifiers

PMID: 20609011
DOI: 10.1111/j.1365-2516.2010.02353.x

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Is hereditary haemorrhagic telangiectasia rare in the black race? The first sub-Saharan mutation.PMID 20609011Read ↗

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European Reference Network for Rare Vascular Diseases (VASCERN) position statement on cerebral screening in adults and children with hereditary haemorrhagic telangiectasia (HHT)Semantic proximity Read ↗

Experience of the Irish National Centre for hereditary haemorrhagic telangiectasia 2003-2008.Semantic proximity Read ↗

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

A disease locus for hereditary haemorrhagic telangiectasia maps to chromosome 9q33–34Semantic proximity Read ↗

Clinical heterogeneity in hereditary haemorrhagic telangiectasia: are pulmonary arteriovenous malformations more common in families linked to endoglin?Semantic proximity Read ↗

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