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Tsc2 mutation rather than Tsc1 mutation dominantly causes a social deficit in a mouse model of tuberous sclerosis complex.
Kashii, Hirofumi; Kasai, Shinya; Sato, Atsushi; Hagino, Yoko; Nishito, Yasumasa; Kobayashi, Toshiyuki; Hino, Okio; Mizuguchi, Masashi; Ikeda, Kazutaka.
Afiliação
  • Kashii H; Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-Ku, Tokyo, 156-8506, Japan.
  • Kasai S; Department of Neuropediatrics, Tokyo Metropolitan Neurological Hospital, 2-6-1 Musashidai, Fuchu, Tokyo, 183-0042, Japan.
  • Sato A; Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-Ku, Tokyo, 156-8506, Japan.
  • Hagino Y; Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-Ku, Tokyo, 156-8506, Japan.
  • Nishito Y; Department of Pediatrics, The University of Tokyo Hospital, 7-3-1 Hongo, Bunkyo-Ku, Tokyo, 113-8655, Japan.
  • Kobayashi T; Addictive Substance Project, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-Ku, Tokyo, 156-8506, Japan.
  • Hino O; Center for Basic Technology Research, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-Ku, Tokyo, 156-8506, Japan.
  • Mizuguchi M; Department of Pathology and Oncology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo, 113-8421, Japan.
  • Ikeda K; Department of Pathology and Oncology, Juntendo University School of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo, 113-8421, Japan.
Hum Genomics ; 17(1): 4, 2023 02 02.
Article em En | MEDLINE | ID: mdl-36732866
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Tuberosa / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals Idioma: En Revista: Hum Genomics Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão
Texto completo
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Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Tuberosa / Transtorno do Espectro Autista Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals Idioma: En Revista: Hum Genomics Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão