Associated Papers
LDLR variant classification through activity-normalized prime editing screening.
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Biorxiv : the Preprint Server for Biology, 2025
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Supplement: media-5.xlsx › SuppTable5
Molecular characterization of Polish patients with familial hypercholesterolemia: novel and recurrent LDLR mutations.
Chmara M et al.
Journal of Applied Genetics, 2010
Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia.
Brusgaard K et al.
Clinical Genetics, 2006
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