Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome.
作者信息
Saitsu Hirotomo, Kato Mitsuhiro, Koide Ayaka, Goto Tomohide, Fujita Takako, Nishiyama Kiyomi, Tsurusaki Yoshinori, Doi Hiroshi, Miyake Noriko, Hayasaka Kiyoshi, Matsumoto Naomichi
出版信息
Ann Neurol. 2012 Aug;72(2):298-300. doi: 10.1002/ana.23620.
PMID:22926866
Abstract
摘要
Zotero 插件