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Journal article 895 views

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
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College: Faculty of Medicine, Health and Life Sciences
Issue: 3
Start Page: 354
End Page: 357