Takako Fujita

Publications (1)11.09 Total impact

• Article: 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 Matsumoto
  Annals of Neurology 08/2012; 72(2):298-300. · 11.09 Impact Factor