Human Glycine a1 -- Ile 244
| Human |
Ile 244 |
Mutations |
|
|
| Rat Equivalent |
Ile 244 |
Mutations |
I244N
| Asn |
| Mouse Equivalent |
Ile 244 |
Mutations |
|
|
hIle244Asn
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
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