SCN1A Gene Mutations in Severe Infantile Myoclonic Epilepsy

Open Access

|Apr 2002

Sugawara T Mazaki-Miyazaki E Fukushima K Shimomura J Fujiwara T Hamano S Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy Neurology 2002 Apr 9 58 7 1122 1124 10.1212/WNL.58.7.1122 11940708
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Language: English

Page range: 28 - 29

Published on: Apr 1, 2002

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

© 2002 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.