Cantu syndrome–associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-of-function by differential mechanisms

Authors

Conor McClenaghan, Washington University School of Medicine in St. Louis
Alex Hanson, Washington University School of Medicine in St. Louis
Monica Sala-Rabanal, Washington University School of Medicine in St. Louis
Helen I. Roessler, Utrecht University
Dragana Josifova, Guy's and St. Thomas NHS Trust
Dorothy K. Grange, Washington University School of Medicine in St. Louis
Gijs van Haaften, Utrecht University
Colin G. Nichols, Washington University School of Medicine in St. Louis

Journal

Journal of Biological Chemistry

Publication Date

2018

Volume

293

Issue

6

Inclusive Pages

2041-2052

Document Type

Open Access Publication

DOI

10.1074/jbc.RA117.000351

Rights and Permissions

This research was originally published in the Journal of Biological Chemistry. McClenaghan C, Hanson A, Sala-Rabanal M, Roessler HI, Josifova D, Grange DK, van Haaften G, Nichols CG. Cantu syndrome-associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-of-function by differential mechanisms. J Biol Chem. 2018 Feb 9;293(6):2041-2052. doi: 10.1074/jbc.RA117.000351. © 2018 by The American Society for Biochemistry and Molecular Biology, Inc.

Recommended Citation

McClenaghan, Conor; Hanson, Alex; Sala-Rabanal, Monica; Roessler, Helen I.; Josifova, Dragana; Grange, Dorothy K.; van Haaften, Gijs; and Nichols, Colin G., "Cantu syndrome–associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-of-function by differential mechanisms." Journal of Biological Chemistry. 293, 6. 2041-2052. (2018).
https://digitalcommons.wustl.edu/open_access_pubs/6587