Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities - support for the role of K(ATP) channels in this condition.

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Published in Eur J Med Genet on October 28, 2013

Authors

Catherine A Brownstein1, Meghan C Towne, Lovelace J Luquette, David J Harris, Nicholas S Marinakis, Peter Meinecke, Kerstin Kutsche, Philippe M Campeau, Timothy W Yu, David M Margulies, Pankaj B Agrawal, Alan H Beggs

Author Affiliations

1: Division of Genetics and Genomics, The Manton Center for Orphan Disease Research, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: catherine.brownstein@childrens.harvard.edu.

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