Mutation screening in patients for familial hypercholesterolaemia (ADH)

Supporting Information Table S1. Mutations identified in the study cohort Mutations in bold are those included in the FH20 ARMs kit Supporting information is available as part of the online article at http://www.blackwell-synergy.com Please note: Wiley-Blackwell Publishing are not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material) should be directed to the corresponding author for the article. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.