Matches in Nanopublications for { ?s ?p "[Autosomal recessive hypercholesterolaemia (ARH), characterized clinically by severe inherited hypercholesterolaemia, is caused by recessive null mutations in LDLRAP1 (formerly ARH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_assertion description "[Autosomal recessive hypercholesterolaemia (ARH), characterized clinically by severe inherited hypercholesterolaemia, is caused by recessive null mutations in LDLRAP1 (formerly ARH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724037.RARo-zW4zt-krjruuVTvhQZ3XomMED1-RXDEqHIrihjVs130_provenance.
- NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_assertion description "[Autosomal recessive hypercholesterolaemia (ARH), characterized clinically by severe inherited hypercholesterolaemia, is caused by recessive null mutations in LDLRAP1 (formerly ARH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921679.RAcw1-rXf23t87eFE1YjlPKvgBVdORCJpxouAxqs5cc28130_provenance.