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Familial hypercholesterolemia: A genetic receptor disease
J. L. Goldstein
,
M. S. Brown
Int Med - Chairman's Office
Molecular Genetics
Internal Medicine
Molecular Genetics
Research output
:
Contribution to journal
›
Article
›
peer-review
13
Scopus citations
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Medicine & Life Sciences
Hyperlipoproteinemia Type II
100%
Homozygote
88%
Heterozygote
86%
Inborn Genetic Diseases
74%
Parturition
56%
Therapeutics
13%