Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome
Hirotomo Saitsu, Mitsuhiro Kato, Ayaka Koide, Tomohide Goto, Takako Fujita, Kiyomi Nishiyama, Yoshinori Tsurusaki, Hiroshi Doi, Noriko Miyake, Kiyoshi Hayasaka, Naomichi MatsumotoVolume:
72
Year:
2012
Language:
english
Pages:
1
DOI:
10.1002/ana.23620
File:
PDF, 88 KB
english, 2012