Paper

Data

Name Claes L, Ceulemans B, Audenaert D, Smets K, Löfgren A, Del-Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P (2003)

Description

Title De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.

References

Authors Claes L Show Other Ceulemans B Show Other Audenaert D Show Other Smets K Show Other Löfgren A Show Other Del-Favero J Show Other Ala-Mello S Show Other Basel-Vanagaite L Show Other Plecko B Show Other Raskin S Show Other Thiry P Show Other Wolf NI Show Other Van Broeckhoven C Show Other De Jonghe P Show Other

Volume 21

First page 615

Last page 21

Publisher

Pubmed ID 12754708

Year published 2003

Month published

Day published

Journal or book name Hum Mutat

Book Editor(s)

Missing References

Type

Digital Object Identifier 10.1002/humu.10217

URL

Stated Usage

Species