Detection of low density lipoprotein receptor gene mutations in patients with familial hypercholesterolaemia / Rafezah Razali

Familial hypercholesterolaemia (FH) is an autosomal dominant inherited disorder of lipoprotein metabolism associated with premature coronary artery disease (CAD). Extrapolating the prevalence of heterozygous FH in western populations into Malaysian population, it would be estimated that about 50,00...

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Bibliographic Details
Main Author:	Rafezah, Razali
Format:	Thesis
Published:	2011
Subjects:	QH301 Biology
Online Access:	http://studentsrepo.um.edu.my/3619/2/1._title_page%2C_abstract%2C_table_of_contents.pdf http://studentsrepo.um.edu.my/3619/3/Chapter_1_Introduction.pdf http://studentsrepo.um.edu.my/3619/4/Chapter_2__Literature_Review.pdf http://studentsrepo.um.edu.my/3619/5/Chapter_3_Materials_%26_Methods.pdf http://studentsrepo.um.edu.my/3619/6/CHAPTER_4__ALL_RESULTS.pdf http://studentsrepo.um.edu.my/3619/7/Chapter_5_Discussion.pdf http://studentsrepo.um.edu.my/3619/8/Chapter_6_Conclusion.pdf http://studentsrepo.um.edu.my/3619/9/Bibliography.pdf http://studentsrepo.um.edu.my/3619/10/Appendices_full.pdf http://pendeta.um.edu.my/client/default/search/results?qu=Detection+of+low+density+lipoprotein+receptor+gene+mutations+in+patients+with+familial+hypercholesterolaemia&te= http://studentsrepo.um.edu.my/3619/
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