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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Main Authors: | , , , , , |
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Format: | Article |
Published: |
2018
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Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/26133 |
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Institution: | Mahidol University |