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NO TO HATTATSU (Official Journal of The Japanese Society of Child Neurology)

Volume 46, Issue 2 / 2014
English Article   Japanese Article
  • Please note that metadata of J-type articlesare generated by machine-translation and the original texts are written in Japanese.
Japanese Article About clinical features associated with condition of a patient understanding - etiology gene (MECP2, CDKL5, FOXG1) mutation of the Rett syndrome―
高橋悟
NO TO HATTATSU (Official Journal of The Japanese Society of Child Neurology) 46(2): 117-120, 2014.
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