Journal article 1034 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 
Epileptic Disorders, Volume: 16, Issue: 3, Pages: 354 - 357
Swansea University Authors:
Mark Rees, Seo-Kyung Chung
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DOI (Published version): 10.1684/epd.2014.0663
Abstract
Neonatal hyperekplexia with homozygous p.R392H mutation in GLRA1.
| Published in: | Epileptic Disorders |
|---|---|
| Published: |
2014
|
| URI: | https://cronfa.swan.ac.uk/Record/cronfa20048 |
| College: |
Faculty of Medicine, Health and Life Sciences |
|---|---|
| Issue: |
3 |
| Start Page: |
354 |
| End Page: |
357 |