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...
Internet
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/3619/2/1._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