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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 Kullmann
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History

Publication status

  • Published

Journal

European Journal Of Neuroscience

ISSN

0953-816X

Publisher

Blackwell Publishing

Issue

2

Volume

16

Page range

186-196

Department affiliated with

  • Neuroscience Publications

Notes

UCL Institute of Neurology, London, UK

Full text available

  • No

Peer reviewed?

  • Yes

Legacy Posted Date

2013-06-14

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