Genomic characterization of five deletions in the LDL receptor gene in Danish Familial Hypercholesterolemic subjects

• Egile Nagusiak: Larsen Mogens L (Egilea), Nielsen Gitte G (Egilea), Stenderup Anette (Egilea), Damgaard Dorte (Egilea), Nissen Peter H (Egilea), Færgeman Ole (Egilea)
• Formatua: Liburua
• Argitaratua: BMC, 2006-06-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Familial Hypercholesterolemia is a common autosomal dominantly inherited disease that is most frequently caused by mutations in the gene encoding the receptor for low density lipoproteins (LDLR). Deletions and other major structural...