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A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency.
Nakatani N, Tamura A, Hanafusa H, Nino N, Yamamoto N, Awano H, Tanaka Y, Morisada N, Uemura S, Saito A, Hasegawa D, Nozu K, Kosaka Y. Nakatani N, et al. Among authors: awano h. Hum Genome Var. 2024 Mar 22;11(1):15. doi: 10.1038/s41439-024-00271-2. Hum Genome Var. 2024. PMID: 38514645 Free PMC article.
Natural history of Becker muscular dystrophy: a multicenter study of 225 patients.
Nakamura A, Matsumura T, Ogata K, Mori-Yoshimura M, Takeshita E, Kimura K, Kawashima T, Tomo Y, Arahata H, Miyazaki D, Takeshima Y, Takahashi T, Ishigaki K, Kuru S, Wakisaka A, Awano H, Funato M, Sato T, Saito Y, Takada H, Sugie K, Kobayashi M, Ozasa S, Fujii T, Maegaki Y, Oi H, Tachimori H, Komaki H. Nakamura A, et al. Among authors: awano h. Ann Clin Transl Neurol. 2023 Dec;10(12):2360-2372. doi: 10.1002/acn3.51925. Epub 2023 Oct 26. Ann Clin Transl Neurol. 2023. PMID: 37882106 Free PMC article.
159 results