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Is phenotype difference in severe myoclonic epilepsy in infancy related to SCN1A mutations?

✍ Scribed by Iori Ohmori; Yoko Ohtsuka; Mamoru Ouchida; Tatsuya Ogino; Satoshi Maniwa; Kenji Shimizu; Eiji Oka

Book ID: 114248986
Publisher: Elsevier Science
Year: 2003
Tongue: English
Weight: 201 KB
Volume: 25
Category: Article
ISSN: 0387-7604
DOI: 10.1016/s0387-7604(03)00038-x

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