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

• Prif Awduron: Larsen Mogens L (Awdur), Nielsen Gitte G (Awdur), Stenderup Anette (Awdur), Damgaard Dorte (Awdur), Nissen Peter H (Awdur), Færgeman Ole (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: BMC, 2006-06-01T00:00:00Z.
• Pynciau: article
• Mynediad Ar-lein: 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...