Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia

• Váldodahkkit: Blanco Francisco J (Dahkki), Garrido-Martin Eva M (Dahkki), Albiñana Virginia (Dahkki), García-Alegria Eva (Dahkki), Fernandez-L Africa (Dahkki), Fontalba Ana (Dahkki), Zarrabeitia Roberto (Dahkki), Perez-Molino Alfonso (Dahkki), Bernabeu-Herrero Maria E (Dahkki), Ojeda Maria-Luisa (Dahkki), Fernandez-Luna Jose L (Dahkki), Bernabeu Carmelo (Dahkki), Botella Luisa M (Dahkki)
• Materiálatiipa: Girji
• Almmustuhtton: BMC, 2008-08-01T00:00:00Z.
• Fáttát: article
• Liŋkkat: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder characterised mainly by mutations in the Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.</p> <p&...