Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia

• Main Authors: Blanco Francisco J (Author), Garrido-Martin Eva M (Author), Albiñana Virginia (Author), García-Alegria Eva (Author), Fernandez-L Africa (Author), Fontalba Ana (Author), Zarrabeitia Roberto (Author), Perez-Molino Alfonso (Author), Bernabeu-Herrero Maria E (Author), Ojeda Maria-Luisa (Author), Fernandez-Luna Jose L (Author), Bernabeu Carmelo (Author), Botella Luisa M (Author)
• Format: Book
• Published: BMC, 2008-08-01T00:00:00Z.
• Subjects: article
• Online Access: 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&...