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Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome

✍ Scribed by Hirotomo Saitsu; Mitsuhiro Kato; Ayaka Koide; Tomohide Goto; Takako Fujita; Kiyomi Nishiyama; Yoshinori Tsurusaki; Hiroshi Doi; Noriko Miyake; Kiyoshi Hayasaka; Naomichi Matsumoto

Book ID: 115549564
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 88 KB
Volume: 72
Category: Article
ISSN: 0364-5134
DOI: 10.1002/ana.23620

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