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 Nature in European Journal of Human Genetics
- Vol. 9 (11) , 873-876
- https://doi.org/10.1038/sj.ejhg.5200729
Abstract
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