Human Glycine a1 -- Ile 244

Human Ile 244 Mutations    
Rat Equivalent Ile 244 Mutations


Mouse Equivalent Ile 244 Mutations    



Rees MI, Andrew M, Jawad S, Owen MJ (1994) Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the alpha 1 subunit of the inhibitory glycine receptor. Human Molecular Genetics 3(12):2175-9

back to top
back to Glycine a1