A recently identified genetic variant for coronary artery disease risk on chromosome 1p13.3 in the region of the PSRC1 and CELSR2 genes associates with serum cholesterol

Braund, P. S. and Erdmann, J. and Tobin, M. D. and Gotz, A. and Tomaszewski, M. and Linsel-Nitschke, P. and Hajat, C. and Hengstenberg, C. and Schunkert, H. and Samani, N. J. (2008) A recently identified genetic variant for coronary artery disease risk on chromosome 1p13.3 in the region of the PSRC1 and CELSR2 genes associates with serum cholesterol. In: ESC Congress 2008, August 30-September 03, 2008, Munich, Germany.

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Item Type: Conference or Workshop Item (UNSPECIFIED)
Subjects: 600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin II
Depositing User: Petra Gürster
Date Deposited: 14 Jul 2022 04:35
Last Modified: 14 Jul 2022 04:35
URI: https://pred.uni-regensburg.de/id/eprint/30344

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