A mutation (V260M) in the middle of the M2 pore-lining domain of the glycine receptor causes hereditary hyperekplexia
- 1 November 2001
- journal article
- research article
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 9 (11), 873-876
- https://doi.org/10.1038/sj.ejhg.5200729