ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating.
Bienengraeber M; Olson TM; Selivanov VA; Kathmann EC; O'Cochlain F; Gao F; Karger AB; Ballew JD; Hodgson DM; Zingman LV; Pang YP; Alekseev AE; Terzic A; Nature Genetics, 2004, vol. 36, issue 4, p 382, ISSN 10614036. ISBN 10614036.

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