Paper

Data

Name Saitsu H, Kato M, Koide A, Goto T, Fujita T, Nishiyama K, Tsurusaki Y, Doi H, Miyake N, Hayasaka K, Matsumoto N (2012)

Description

Title Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.

References

Authors Saitsu H Show Other Kato M Show Other Koide A Show Other Goto T Show Other Fujita T Show Other Nishiyama K Show Other Tsurusaki Y Show Other Doi H Show Other Miyake N Show Other Hayasaka K Show Other Matsumoto N Show Other

Volume 72

First page 298

Last page 300

Publisher

Pubmed ID 22926866

Year published 2012

Month published

Day published

Journal or book name Ann Neurol

Book Editor(s)

Missing References

Type

Digital Object Identifier 10.1002/ana.23620

URL

Stated Usage

Species