Matches in DBpedia 2016-04 for { ?s ?p "Apolipoprotein B deficiency (also known as \"Familial defective apolipoprotein B-100\") is an autosomal dominant disorder resulting from a missense mutation which reduces the affinity of apoB-100 for the low-density lipoprotein receptor (LDL Receptor) (see native LDL-ApoB structure at 37°C on YouTube) . This causes impairments in LDL catabolism, resulting in increased levels of low-density lipoprotein in the blood. The clinical manifestations are similar to diseases produced by mutations of the LDL receptor, such as familial hypercholesterolemia. Treatment may include, niacin or statin or ezetimibe.It is also known as \"normotriglyceridemic hypobetalipoproteinemia\"."@en }
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- Apolipoprotein_B_deficiency abstract "Apolipoprotein B deficiency (also known as \"Familial defective apolipoprotein B-100\") is an autosomal dominant disorder resulting from a missense mutation which reduces the affinity of apoB-100 for the low-density lipoprotein receptor (LDL Receptor) (see native LDL-ApoB structure at 37°C on YouTube) . This causes impairments in LDL catabolism, resulting in increased levels of low-density lipoprotein in the blood. The clinical manifestations are similar to diseases produced by mutations of the LDL receptor, such as familial hypercholesterolemia. Treatment may include, niacin or statin or ezetimibe.It is also known as \"normotriglyceridemic hypobetalipoproteinemia\".".