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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Published on: August 8, 2022

Genetic variation in ABCG1 and risk of myocardial infarction and ischemic heart disease

Jesper Schou1, Ruth Frikke-Schmidt, Dimitris Kardassis

  • 1Department of Clinical Biochemistry KB3011, Section for Molecular Genetics, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, DK-2100 Copenhagen, Denmark.

Arteriosclerosis, Thrombosis, and Vascular Biology
|December 14, 2011
PubMed
Abstract

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