Paper

Data

Name Berecki G, Bryson A, Terhag J, Maljevic S, Gazina EV, Hill SL, Petrou S (2019)

Description

Title SCN1A gain of function in early infantile encephalopathy.

References

Authors Petrou S Show Other Hill SL Show Other Gazina EV Show Other Maljevic S Show Other Berecki G Show Other Bryson A Show Other Terhag J Show Other

Volume 85

First page 514

Last page 525

Publisher

Pubmed ID 30779207

Year published 2019

Month published

Day published

Journal or book name Ann Neurol

Book Editor(s)

Missing References Claes L, Del-Favero J, Ceulemans B, et al. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet 2001; 68: 1327– 1332. <| [No Pubmed ID Found] |>

Type

Digital Object Identifier 10.1002/ana.25438

URL

Stated Usage

Species