Pages that link to "Q43136172"

The following pages link to Identification of a recurrent insertion mutation in the LDLR gene in a Pakistani family with autosomal dominant hypercholesterolemia (Q43136172):

Displaying 7 items.

• Novel and recurrent LDLR gene mutations in Pakistani hypercholesterolemia patients (Q30412645) (← links)
• Elevated PLA2G7 gene promoter methylation as a gender-specific marker of aging increases the risk of coronary heart disease in females (Q34652118) (← links)
• The genetic spectrum of familial hypercholesterolemia in Pakistan (Q36983501) (← links)
• Familial hypercholesterolemia: epidemiology, Neolithic origins and modern geographic distribution (Q37887013) (← links)
• Synergism between paraoxonase Arg 192 and the angiotensin converting enzyme D allele is associated with severity of coronary artery disease. (Q54364291) (← links)
• Paraoxonase Arg 192 allele is an independent risk factor for three-vessel stenosis of coronary artery disease (Q62071577) (← links)
• Decreased serum PON1 arylesterase activity in familial hypercholesterolemia patients with a mutated LDLR gene (Q90465328) (← links)