Whole Exome Sequencing Implicates an INO80D Mutation in a Syndrome of Aortic Hypoplasia, Premature Atherosclerosis, and Arterial Stiffness
Circulation: Cardiovascular Genetics
doi 10.1161/circgenetics.113.000233
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Date
October 1, 2014
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Ovid Technologies (Wolters Kluwer Health)