Mutation analysis of <it>"Endoglin" </it>and <it>"Activin receptor-like kinase" </it>genes in German patients with hereditary hemorrhagic telangiectasia and the value of rapid genotyping using an allele-specific PCR-technique
<p>Abstract</p> <p>Background</p> <p>Hereditary hemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is an autosomal dominant disorder which is clinically characterised by recurrent epistaxis, mucocutaneous telangiectasia and visceral arteriovenou...
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| Main Authors: | , , , , , , |
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| Format: | Book |
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BMC,
2009-06-01T00:00:00Z.
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