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Whole exome sequencing identifies KCNQ2 mutations in Ohtahara syndrome
Author(s) -
Saitsu Hirotomo,
Kato Mitsuhiro,
Koide Ayaka,
Goto Tomohide,
Fujita Takako,
Nishiyama Kiyomi,
Tsurusaki Yoshinori,
Doi Hiroshi,
Miyake Noriko,
Hayasaka Kiyoshi,
Matsumoto Naomichi
Publication year - 2012
Publication title -
annals of neurology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 4.764
H-Index - 296
eISSN - 1531-8249
pISSN - 0364-5134
DOI - 10.1002/ana.23620
Subject(s) - medical school , pediatric neurology , medicine , library science , medical education , pediatrics , computer science
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