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Correction: Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.
Yaoita H, Kawai E, Takayama J, Iwasawa S, Saijo N, Abiko M, Suzuki K, Kimura M, Ozawa A, Tamiya G, Kure S, Kikuchi A. Yaoita H, et al. Among authors: saijo n. J Hum Genet. 2024 May;69(5):185. doi: 10.1038/s10038-024-01245-6. J Hum Genet. 2024. PMID: 38548934 Free PMC article. No abstract available.
Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.
Yaoita H, Kawai E, Takayama J, Iwasawa S, Saijo N, Abiko M, Suzuki K, Kimura M, Ozawa A, Tamiya G, Kure S, Kikuchi A. Yaoita H, et al. Among authors: saijo n. J Hum Genet. 2024 May;69(5):177-183. doi: 10.1038/s10038-024-01223-y. Epub 2024 Feb 13. J Hum Genet. 2024. PMID: 38351237 Free PMC article.
Treatment of ZC4H2 Variant-Associated Spastic Paraplegia with Selective Dorsal Rhizotomy and Intensive Postoperative Rehabilitation: A Case Report.
Inotani T, Horaguchi A, Morishita Y, Yoshida A, Otomo M, Suzuki M, Inui T, Okubo Y, Komatsu S, Mizuno C, Takahashi Y, Ochiai T, Kinjo T, Asato T, Takayama J, Tamiya G, Saijo N, Kikuchi A, Haginoya K. Inotani T, et al. Among authors: saijo n. Tohoku J Exp Med. 2024 Apr 24;262(4):239-244. doi: 10.1620/tjem.2024.J004. Epub 2024 Jan 25. Tohoku J Exp Med. 2024. PMID: 38267061 Free article.
[History of the Japanese Society of Medical Oncology].
Ishioka C, Minami H, Ohe Y, Tamura K, Saijo N. Ishioka C, et al. Among authors: saijo n. Gan To Kagaku Ryoho. 2024 Jan;51(1):45-52. Gan To Kagaku Ryoho. 2024. PMID: 38247091 Review. Japanese.
Highly reproducible eyeblink timing during formula car driving.
Nishizono R, Saijo N, Kashino M. Nishizono R, et al. Among authors: saijo n. iScience. 2023 May 19;26(6):106803. doi: 10.1016/j.isci.2023.106803. eCollection 2023 Jun 16. iScience. 2023. PMID: 37378324 Free PMC article.
755 results