Analysis of the human KCNH2(HERG) gene: identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion.

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Published in Hum Mutat on May 01, 2000

Authors

A Paulussen1, P Yang, M Pangalos, P Verhasselt, R Marrannes, C Verfaille, I Vandenberk, R Crabbe, F Konings, W Luyten, M Armstrong

Author Affiliations

1: Department of Pharmacogenomics, Janssen Research Foundation, Janssen Pharmaceutica, Belgium.

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