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Paper Details

Clinical characterization of familial hypercholesterolemia due to an amish founder mutation in Apolipoprotein B.
BMC Cardiovasc Disord
3
2022
ApoB, ApoB heterozygotes, Apolipoprotein B, FH, Familial hypercholesterolemia, LDL, LDL cholesterol, LDL particles, LDL-C, LDL-P, atherosclerosis, atherosclerotic plaque, children, cholesterol, familial hypercholesterolemia
Author NameAffiliation
Millie YoungClinic for Special Children
Erik G PuffenbergerClinic for Special Children
Karlla W BrigattiClinic for Special Children
Alan R ShuldinerRegeneron Pharmaceuticals Inc.
Alan R ShuldinerRegeneron Pharmaceuticals Inc.
Kevin A StraussClinic for Special Children
Kevin A StraussPenn Medicine-Lancaster General Hospital
Devyani ChowdhuryNemours Alfred I. duPont Hospital for Children
Devyani ChowdhuryPenn Medicine-Lancaster General Hospital
Devyani Chowdhury
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