A rare genetic variant in the cleavage site of prepro-orexin confers susceptibility to idiopathic hypersomnia

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Authors: T. Miyagawa, S. Tanaka, M. Shimada, Noriaki Sakai, Kotomi Tanida, N. Kotorii, Tatayu Kotorii, Y. Ariyoshi, Y. Hashizume, Kimihiro Ogi, Hiroshi Hiejima, T. Kanbayashi
+32 more Aya Imanishi, Azusa Ikegami, Y. Kamei, A. Hida, Y. Wada, M. Miyamoto, M. Takami, H. Kondo, Y. Tamura, Y. Taniyama, N. Omata, T. Mizuno, S. Moriya, H. Furuya, M. Kato, K. Kato, J. Ishigooka, K. Tsuruta, Shintaro Chiba, N. Yamada, M. Okawa, Koichi Hirata, K. Kuroda, K. Kume, N. Uchimura, M. Kitada, T. Kodama, Y. Inoue, Seiji Nishino, K. Mishima, K. Tokunaga, M. Honda
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Fields of Study & Subjects

Sleep and Wakefulness Research Sleep and related disorders Obstructive Sleep Apnea Research

Publication details

Journal / source
Sleep Medicine
Volume
138
Pages
107227–107227
Publication date
29 January 2026
Language
EN