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Neonatal hyperekplexia with homozygous p.R392H mutation in GLRA1.

F. Hmami, S.E. Wood, S. Chaouki, A. Oulmaati, M. Hida, M.I. Rees, S.K. Chung, A. Bouharrou, Mark Rees, Seo-Kyung Chung Orcid Logo

Epileptic Disorders, Volume: 16, Issue: 3, Pages: 354 - 357

Swansea University Authors: Mark Rees, Seo-Kyung Chung Orcid Logo

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DOI (Published version): 10.1684/epd.2014.0663

Published in: Epileptic Disorders
Published: 2014
URI: https://cronfa.swan.ac.uk/Record/cronfa20048
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College: Swansea University Medical School
Issue: 3
Start Page: 354
End Page: 357