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."@en }
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- Apolipoprotein_B_deficiency comment "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.".