Contribution of germline and somatic mutations to risk of neuromyelitis optica spectrum disorder.
Yata T, Sato G, Ogawa K, Naito T, Sonehara K, Saiki R, Edahiro R, Namba S, Watanabe M, Shirai Y, Yamamoto K, NamKoong H, Nakanishi T, Yamamoto Y, Hosokawa A, Yamamoto M; Japan MS/NMOSD biobank; BioBank Japan Project; Japan COVID-19 Task Force; Oguro-Igashira E, Nii T, Maeda Y, Nakajima K, Nishikawa R, Tanaka H, Nakayamada S, Matsuda K, Nishigori C, Sano S, Kinoshita M, Koike R, Kimura A, Imoto S, Miyano S, Fukunaga K, Mihara M, Shimizu Y, Kawachi I, Miyamoto K, Tanaka Y, Kumanogoh A, Niino M, Nakatsuji Y, Ogawa S, Matsushita T, Kira JI, Mochizuki H, Isobe N, Okuno T, Okada Y.
Yata T, et al. Among authors: namkoong h.
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Cell Genom. 2025.
PMID: 39986280
Free PMC article.