Literature DB >> 17046772

H3543Y mutation of apoB-100 in patients with phenotype of familial hypercholesterolemia.

Zuzana Basistová, Juraj Gasparovic, Daniela Siváková, Katarína Raslová.   

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Year:  2006        PMID： 17046772     DOI： 10.1016/j.atherosclerosis.2006.08.055

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN： 0021-9150            Impact factor:   5.162


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  1 in total

1.  A Rare Double Heterozygous Mutation in Low-Density Lipoprotein Receptor and Apolipoprotein B-100 Genes in a Severely Affected Familial Hypercholesterolaemia Patient.

Authors:  Lilla Juhász; István Balogh; László Madar; Beáta Kovács; Mariann Harangi
Journal:  Cureus       Date:  2020-12-20
  1 in total

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