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

• Үндсэн зохиолчид: Haneen Sadick (Зохиогч), Johanna Hage (Зохиогч), Ulrich Goessler (Зохиогч), Jens Stern-Straeter (Зохиогч), Frank Riedel (Зохиогч), Karl Hoermann (Зохиогч), Peter Bugert (Зохиогч)
• Формат: Ном
• Хэвлэсэн: BMC, 2009-06-01T00:00:00Z.
• Нөхцлүүд: article
• Онлайн хандалт: Connect to this object online.

<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...