Associated Papers
Recapitulating familial hypercholesterolemia in a mouse model by knock-in patient-specific LDLR mutation.
Liu J et al.
Faseb Journal : Official Publication of the Federation of American Societies for Experimental Biology, 2024
Joint genotypic and phenotypic outcome modeling improves base editing variant effect quantification.
Ryu J et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
37732177 (PubMed )
Supplement: media-3.zip › Supplementary_Tables › TableS8_features_full_struc.xlsx › in
The LDLR, APOB, and PCSK9 Variants of Index Patients with Familial Hypercholesterolemia in Russia.
Meshkov A et al.
Genes, 2021
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