A rare variant in MCF2L identified using exclusion linkage...

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European Journal of Human Genetics 2015 / 04

A rare variant in MCF2L identified using exclusion linkage in a pedigree with premature atherosclerosis

Maiwald, Stephanie, Motazacker, Mahdi M, van Capelleveen, Julian C, Sivapalaratnam, Suthesh, van der Wal, Allard C, van der Loos, Chris, Kastelein, John J P, Ouwehand, Willem H, Hovingh, G Kees, Trip,
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Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2015.70
Date:
April, 2015
File:
PDF, 1.55 MB
english, 2015
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