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M.597 Characterisation of the low density lipoprotein receptor gene mutations causing familial hyperholesterolaemia in Northwestern Greece

โœ Scribed by Miltiadous, G.; Xenophontos, S.; Tsimihodimos, V.; Cariolou, M.; Elisaf, M.


Book ID
118632989
Publisher
Elsevier Science
Year
2004
Tongue
English
Weight
150 KB
Volume
5
Category
Article
ISSN
1567-5688

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Familial Hypercholesterolaemia (FH) is a clinical syndrome characterised by elevated serum total cholesterol levels due to an increase in low density lipoprotein (LDL) cholesterol, by tendon xanthomata and clinical manifestations of ischaemic heart disease in early life. Typically, it results from m