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Functional characterization of compound heterozygosity for GlyRa1 mutations in the startle disease hyperekplexia
journal contribution
posted on 2023-06-08, 15:14 authored by Ruth Rea, Marina A Tijssen, Colin Herd, Rune R Frants, Dimitri M KullmannNo description supplied
History
Publication status
- Published
Journal
European Journal Of NeuroscienceISSN
0953-816XPublisher
Blackwell PublishingExternal DOI
Issue
2Volume
16Page range
186-196Department affiliated with
- Neuroscience Publications
Notes
UCL Institute of Neurology, London, UKFull text available
- No
Peer reviewed?
- Yes
Legacy Posted Date
2013-06-14Usage metrics
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