Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome

• Hiroshi Maeda

• Tomohiro Chiyonobu

• Michiko Yoshida

• Satoshi Yamashita

• Masashi Zuiki

• Satoshi Kidowaki

• Kenichi Isoda

• Kazuhiro Yamakawa

• Masafumi Morimoto

• Tatsutoshi Nakahata

• Megumu K Saito

• Hajime Hosoi

収録刊行物

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 61 (6), 565-569, 2016-06

  Tokyo : Springer Nature

詳細情報

• CRID: 1523388079932820608
• NII論文ID: 40020857171
• NII書誌ID: AA11206160
• ISSN: 14345161
• NDL書誌ID: 027433533
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I027433533
• 本文言語コード: en
• NDL 雑誌分類:
  • ZS16(科学技術--医学--人類遺伝学)
• データソース種別:
  • NDL
  • CiNii Articles