The Startle Disease Mutation E103K Impairs Activation of Human Homomeric α1 Glycine Receptors by Disrupting an Intersubunit Salt Bridge across the Agonist Binding Site

Fatemah Safar, Elliot Hurdiss, Marios Erotocritou, Timo Greiner, Remigijus Lape, Mark W. Irvine, Guang Y Fang, David Jane, Rilei Yu, Marc A. Dämgen, Philip C. Biggin, Lucia G. Sivilotti*

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)

4 Citations (Scopus)
263 Downloads (Pure)

Fingerprint Dive into the research topics of 'The Startle Disease Mutation E103K Impairs Activation of Human Homomeric α1 Glycine Receptors by Disrupting an Intersubunit Salt Bridge across the Agonist Binding Site'. Together they form a unique fingerprint.

Medicine & Life Sciences