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The contribution of rare genetic variants to the heritability of myocardial infarction: Systematic functional characterization of LDL-Receptor missense alleles identified through exome sequencing of large clinical cohorts

Thormählen, Aenne Solvejg

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Citation of documents: Please do not cite the URL that is displayed in your browser location input, instead use the DOI, URN or the persistent URL below, as we can guarantee their long-time accessibility.
Document type: Abstract of a medical dissertation
Supervisor: Runz, Dr. med. Heiko
Date of thesis defense: 17 May 2017
Date Deposited: 29 Jun 2017 07:43
Date: 2017
Faculties / Institutes: Medizinische Fakultät Heidelberg > Institut für Humangenetik
DDC-classification: 610 Medical sciences Medicine
Uncontrolled Keywords: Humangenetik
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