المؤلفون: Shimomura, Rina^{Aff1, Aff2}, Yanagishita, Tomoe, Ishiguro, Kumiko, Shichiji, Minobu, Sato, Takatoshi, Shimojima Yamamoto, Keiko^{Aff3, Aff4}, Nagata, Miho, Ishihara, Yasuki, Miyashita, Yohei^{Aff5, Aff6}, Ishigaki, Keiko, Nagata, Satoru, Asano, Yoshihiro^{Aff5, Aff6}, Yamamoto, Toshiyuki^{Aff2, Aff4, IDs41439023002629_cor13}

المصدر: Human Genome Variation. 11(1)

المؤلفون: Shimojima Yamamoto, Keiko, Shimomura, Rina, Shoji, Hiromichi, Yamamoto, Toshiyuki

المصدر: In Brain and Development October 2024 46(9):281-285

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المؤلفون: Shimomura R; Department of Pediatrics, School of Medicine, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan., Ito S; Department of Pediatrics, School of Medicine, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan., Kurotaki N; Department of Clinical Psychology, Faculty of Medicine, Graduate School of Medicine, Kagawa University, Kita-gun, Kagawa, Japan., Saito K; Institute of Medical Genetics, School of Medicine, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan., Nagata S; Department of Pediatrics, School of Medicine, Tokyo Women's Medical University, Shinjuku-ku, Tokyo, Japan.

المصدر: Pediatrics international : official journal of the Japan Pediatric Society [Pediatr Int] 2022 Jan; Vol. 64 (1), pp. e14681. Date of Electronic Publication: 2021 Sep 07.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 100886002 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1442-200X (Electronic) Linking ISSN: 13288067 NLM ISO Abbreviation: Pediatr Int Subsets: MEDLINE

مواضيع طبية MeSH: Epilepsy, Benign Neonatal*, Child ; Humans ; Mutation ; Pedigree ; Seizures/diagnosis ; Seizures/etiology