A novel mutation in exon 5 of the low density lipoprotein receptor gene in a Malay family with familial hypercholesterolaemia (FH)

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A novel mutation in exon 5 of the low density lipoprotein receptor gene in a Malay family with familial hypercholesterolaemia (FH)

F�amilial hypercholesterolaemia (FH) is an autosomal dominant inherited disease of lipid metabolism caused by mutations in the low density lipoprotein receptor (LDLR) gene. FH is clinically characterised by an elevated concentration of total cholesterol (TC) and low density lipoprotein cholesterol (...

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Bibliographic Details
Main Authors:	Abdul Murad N. A., Hapizah M. N., Khalid Y., Khalid BAK, Jamal R.
Format:	Article
Language:	English
Published:	Pusat Perubatan Universiti Kebangsaan Malaysia 2013
Online Access:	http://journalarticle.ukm.my/13235/ http://journalarticle.ukm.my/13235/1/8-14-1-SM.pdf

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