Functional characterization of a novel KCNJ11 in frame mutation-deletion associated with infancy-onset diabetes and a mild form of intermediate DEND: A battle between K(ATP) gain of channel activity and loss of channel expression

Authors

Yu-Wen Lin, Washington University School of Medicine in St. Louis
Anlong Li, Washington University School of Medicine in St. LouisFollow
Valerie Grasso, University of Tor Vergata, Rome
Domenica Battaglia, Sacro Cuore Catholic University, Rome
Antonino Crino, Bambino Gesu` Children’s Hospital, Research Institute, Palidoro, Rome
Carlo Colombo, University of Tor Vergata, Rome
Fabrizio Barbetti, University of Tor Vergata, Rome
Colin G. Nichols, Washington University School of Medicine in St. Louis

Journal

PLoS One

Publication Date

2013

Volume

8

Issue

5

Inclusive Pages

e63758

Document Type

Open Access Publication

DOI

10.1371/journal.pone.0063758

Rights and Permissions

Lin Y-W, Li A, Grasso V, Battaglia D, Crinò A, et al. (2013) Functional Characterization of a Novel KCNJ11 in Frame Mutation-Deletion Associated with Infancy-Onset Diabetes and a Mild Form of Intermediate DEND: A Battle between KATP Gain of Channel Activity and Loss of Channel Expression. PLoS ONE 8(5): e63758. doi:10.1371/journal.pone.0063758

Recommended Citation

Lin, Yu-Wen; Li, Anlong; Grasso, Valerie; Battaglia, Domenica; Crino, Antonino; Colombo, Carlo; Barbetti, Fabrizio; and Nichols, Colin G., "Functional characterization of a novel KCNJ11 in frame mutation-deletion associated with infancy-onset diabetes and a mild form of intermediate DEND: A battle between K(ATP) gain of channel activity and loss of channel expression." PLoS One. 8, 5. e63758. (2013).
https://digitalcommons.wustl.edu/open_access_pubs/1499