Publication not explained
Read the Original
This page is a summary of: The Startle Disease Mutation Q266H, in the Second Transmembrane Domain of the Human Glycine Receptor, Impairs Channel Gating, Molecular Pharmacology, February 1999, American Society for Pharmacology & Experimental Therapeutics (ASPET), DOI: 10.1124/mol.55.2.386.
You can read the full text:
Be the first to contribute to this page