Pages that link to "Q82858845"
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The following pages link to Human lecithin:cholesterol acyltransferase deficiency: in vivo kinetics of low-density lipoprotein and lipoprotein-X (Q82858845):
Displaying 6 items.
- Lipoprotein X Causes Renal Disease in LCAT Deficiency (Q28550403) (← links)
- Two novel mutations of lecithin:cholesterol acyltransferase (LCAT) gene and the influence of APOE genotypes on clinical manifestations (Q35574596) (← links)
- Familial lecithin:cholesterol acyltransferase deficiency: First-in-human treatment with enzyme replacement (Q36783281) (← links)
- Systemic and renal lipids in kidney disease development and progression (Q37148885) (← links)
- Lecithin cholesterol acyltransferase: an anti- or pro-atherogenic factor? (Q37224981) (← links)
- Novel Missense LCAT Gene Mutation Associated with an Atypical Phenotype of Familial LCAT Deficiency in Two Portuguese Brothers (Q49566406) (← links)