Paper

Data

Name Vanmolkot KR, Babini E, de Vries B, Stam AH, Freilinger T, Terwindt GM, Norris L, Haan J, Frants RR, Ramadan NM, Ferrari MD, Pusch M, van den Maagdenberg AM, Dichgans M (2007)

Description

Title The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online.

References

Authors Vanmolkot KR Show Other Babini E Show Other de Vries B Show Other Stam AH Show Other Freilinger T Show Other Terwindt GM Show Other Norris L Show Other Haan J Show Other Frants RR Show Other Ramadan NM Show Other Ferrari MD Show Other Pusch M Show Other van den Maagdenberg AM Show Other Dichgans M Show Other

Volume 28

First page 522

Last page

Publisher

Pubmed ID 17397047

Year published 2007

Month published

Day published

Journal or book name Hum Mutat

Book Editor(s)

Missing References

Type

Digital Object Identifier 10.1002/humu.9486

URL

Stated Usage

Species