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. - Paulina

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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.

scientific article

Author/s

author: Antonino Crinò, Fabrizio Barbetti

Work details

Publication date

May 7, 2013

Language

English

Copyright status

copyrighted