Genetics and epigenetics of rare hypersomnia.

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第一作者： Maria Paola,Mogavero

第一单位： Vita-Salute San Raffaele University, Milan, Italy; Sleep Disorders Center, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy.

作者： Maria Paola,Mogavero ^[1] ; Lourdes M,DelRosso ^[2] ; Oliviero,Bruni ^[3] ; Michele,Salemi ^[4] ; Maria,Salsone ^[5] ; Fabiana,Novellino ^[6] ; Marco,Zucconi ^[7] ; Luigi,Ferini Strambi ^[1] ; Raffaele,Ferri ^[8]

作者单位： Vita-Salute San Raffaele University, Milan, Italy; Sleep Disorders Center, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy. ^[1] Seattle Children's Hospital and University of Washington, Seattle, WA, USA. ^[2] Developmental and Social Psychology, Sapienza University of Rome, Rome, Italy. ^[3] Oasi Research Institute - IRCCS, Troina, Italy. ^[4] Vita-Salute San Raffaele University, Milan, Italy; Institute of Molecular Bioimaging and Physiology, National Research Council, Milan, Italy. ^[5] Institute of Molecular Bioimaging and Physiology, National Research Council, Catanzaro, Italy. ^[6] Sleep Disorders Center, Division of Neuroscience, San Raffaele Scientific Institute, Milan, Italy. ^[7] Oasi Research Institute - IRCCS, Troina, Italy. Electronic address: rferri@oasi.en.it. ^[8]

关键词 Kleine–Levin syndrome central disorders of hypersomnolence epigenetics genetics idiopathic hypersomnia narcolepsy type 1 narcolepsy type 2 rare hypersomnia

主题词人类(Humans);过度嗜睡性障碍(Disorders of Excessive Somnolence);发作性睡病(Narcolepsy);后成说, 遗传(Epigenesis, Genetic)

DOI 10.1016/j.tig.2023.02.003

PMID 36842900

发布时间 2023-05-21

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