Associated Papers
The molecular basis of familial hypercholesterolemia in the Czech Republic: spectrum of LDLR mutations and genotype-phenotype correlations.
Tichý L et al.
Atherosclerosis, 2012
An APEX-based genotyping microarray for the screening of 168 mutations associated with familial hypercholesterolemia.
Dušková L et al.
Atherosclerosis, 2011
The UMD-LDLR database: additions to the software and 490 new entries to the database.
Villéger L et al.
Human Mutation, 2002
Spectrum of low density lipoprotein receptor mutations in Czech hypercholesterolemic patients.
Kuhrová V et al.
Human Mutation, 2002
Spectrum of low density lipoprotein receptor mutations in Czech hypercholesterolemic patients.
Kuhrová V et al.
Human Mutation, 2001
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