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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URN: urn:nbn:de:bsz:16-heidok-231594
URL: http://www.ub.uni-heidelberg.de/archiv/23159

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