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Txn1 mutation causes epilepsy associated with vacuolar degeneration in the midbrain
View ORCID ProfileIori Ohmori, Mamoru Ouchida, Hirohiko Imai, Saeko Ishida, Shinya Toyokuni, Tomoji Mashimo
doi: https://doi.org/10.1101/2021.10.07.463470
Iori Ohmori
1Section of Developmental Physiology and Pathology, Education, Institute of Academic and Research, Okayama University, Tsushima 3-chome 1-1, Kita-ku, Okayama 700-8530, Japan
2Department of Child Neurology, Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Shikatacho 2-chome 5-1, Kita-Ku, Okayama 700-8558, Japan
Mamoru Ouchida
3Department of Molecular Oncology, Medicine, Dentistry and Pharmaceutical Sciences, Institute of Academic and Research, Okayama University, Shikatacho 2-Chome 5-1, Kita-Ku, Okayama 700-8558, Japan
Hirohiko Imai
4Department of Systems Science, Kyoto University Graduate School of Informatics, Yoshida-Honmachi, Sakyo-ward, Kyoto 606-8501, Japan
Saeko Ishida
5Division of Animal Genetics, Laboratory Animal Research Center, Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan
Shinya Toyokuni
6Department of Pathology and Biological Responses, Nagoya University Graduate School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya 466-8550, Japan
Tomoji Mashimo
5Division of Animal Genetics, Laboratory Animal Research Center, Institute of Medical Science, The University of Tokyo, Tokyo, 108-8639, Japan
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Posted October 09, 2021.
Txn1 mutation causes epilepsy associated with vacuolar degeneration in the midbrain
Iori Ohmori, Mamoru Ouchida, Hirohiko Imai, Saeko Ishida, Shinya Toyokuni, Tomoji Mashimo
bioRxiv 2021.10.07.463470; doi: https://doi.org/10.1101/2021.10.07.463470
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