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Mutations causative of familial hypercholesterolaemia: sc... | ResearchHub
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Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217
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Authors
Marianne Benn
3 more
Marianne Benn
•
Gerald Watts
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•
Børge Nordestgaard
Published
February 22, 2016
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Journal
European Heart Journal
Topics
Biology
Internal Medicine
Medicine
Endocrinology
Surgery
Show all topics
DOI
10.1093/eurheartj/ehw028
