Mutation analysis of exon 9 of the LDL receptor gene in Thai subjects with primary hypercholesterolemia

The low density lipoprotein (LDL) receptor plays an important role in cholesterol homeostasis. A mutation in this gene causes an autosomal codominant disorder, namely familial hypercholesterolemia (FH). In this study, single strand conformation polymorphism (SSCP) analysis was used to screen for mut...

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Bibliographic Details
Main Authors: Preyanuj Yamwong, Klai Upsorn S. Pongrapeeporn, Pikun Thepsuriyanont, Anchalee Amornrattana, Anchaleekorn Somkasettrin, Kosit Sribhen
Other Authors: Mahidol University
Format: Article
Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/26133
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Institution: Mahidol University