Publication | Closed Access
Identification of a heterozygous compound individual with familial hypercholesterolemia and familial defective apolipoprotein B-100
20
Citations
21
References
1991
Year
Familial HypercholesterolemiaLipid DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyHeterozygous Compound IndividualPathologyLipoprotein MetabolismMedicineAtherosclerosisDyslipidemia
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