Sar1-GTPase-dependent ER exit of KATP channels revealed by a mutation causing congenital hyperinsulinism. [electronic resource]
- Human molecular genetics Jul 2009
- 2400-13 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1460-2083
10.1093/hmg/ddp179 doi
Amino Acid Motifs Amino Acid Sequence Cell Line Congenital Hyperinsulinism--genetics Endoplasmic Reticulum--genetics Humans Insulin--metabolism Insulin Secretion KATP Channels--genetics Molecular Sequence Data Monomeric GTP-Binding Proteins--genetics Mutation, Missense Potassium Channels, Inwardly Rectifying--chemistry Protein Binding Protein Transport Sequence Alignment