Identification of a common low density lipoprotein receptor mutation (C163Y) in the west of Scotland.

Familial hypercholesterolaemia (FH) is an autosomal codominant disorder characterised by high levels of LDL cholesterol and a high incidence of coronary artery disease. Our aims were to track the low density lipoprotein receptor (LDLR) gene in individual families with phenotypic FH and to identify a...

Descrición completa

Gardado en:
Detalles Bibliográficos
Main Authors: Lee, W K, Haddad, L, Macleod, M J, Dorrance, A M, Wilson, D J, Gaffney, D, Dominiczak, M H, Packard, C J, Day, I N, Humphries, S E, Dominiczak, A F
Formato: Artigo
Idioma:Inglês
Publicado: 1998
Assuntos:
Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051368/
https://ncbi.nlm.nih.gov/pubmed/9678702
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares