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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...

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Dettagli Bibliografici
Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: 1998
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1051368/
https://ncbi.nlm.nih.gov/pubmed/9678702
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