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...

وصف كامل

محفوظ في:

التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Rafezah, Razali
التنسيق:	أطروحة
منشور في:	2011
الموضوعات:	QH301 Biology
الوصول للمادة أونلاين:	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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