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

Research output: Contribution to journal › Article › Academic › peer-review

Original language	English
Pages (from-to)	86-91
Journal	European journal of human genetics
Volume	24
Issue number	1
DOIs	https://doi.org/10.1038/ejhg.2015.70
Publication status	Published - 2016

ID: 2611623