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Page 1
Ubap1 knock-in mice reproduced the phenotype of SPG80.
Shimozono K, Nan H, Hata T, Saito K, Kim YJ, Nagatomo H, Ohtsuka T, Koizumi S, Takiyama Y. Shimozono K, et al. Among authors: hata t. J Hum Genet. 2022 Dec;67(12):679-686. doi: 10.1038/s10038-022-01073-6. Epub 2022 Aug 12. J Hum Genet. 2022. PMID: 35962060 Free PMC article.
A clinical and genetic study of SPG31 in Japan.
Hata T, Nan H, Koh K, Ishiura H, Tsuji S, Takiyama Y. Hata T, et al. J Hum Genet. 2022 Jul;67(7):421-425. doi: 10.1038/s10038-022-01021-4. Epub 2022 Feb 7. J Hum Genet. 2022. PMID: 35132160
RFC1 repeat expansion in Japanese patients with late-onset cerebellar ataxia.
Tsuchiya M, Nan H, Koh K, Ichinose Y, Gao L, Shimozono K, Hata T, Kim YJ, Ohtsuka T, Cortese A, Takiyama Y. Tsuchiya M, et al. Among authors: hata t. J Hum Genet. 2020 Dec;65(12):1143-1147. doi: 10.1038/s10038-020-0807-x. Epub 2020 Jul 21. J Hum Genet. 2020. PMID: 32694621
[A case of ataxic gait disturbance due to 1-bromopropane neurotoxicity].
Morishima Y, Fukao T, Tsuchiya M, Hata T, Shindo K, Takiyama Y. Morishima Y, et al. Among authors: hata t. Rinsho Shinkeigaku. 2023 Jan 28;63(1):27-30. doi: 10.5692/clinicalneurol.cn-001799. Epub 2022 Dec 24. Rinsho Shinkeigaku. 2023. PMID: 36567103 Japanese.
26 results