Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Cushing Syndrome and ARMC5[original query] |
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ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers. Journal of the Endocrine Society 2019 9 3 (10): 1837-1846. Kyo Chika, Usui Takeshi, Kosugi Rieko, Torii Mizuki, Yonemoto Takako, Ogawa Tatsuo, Kotani Masato, Tamura Naohisa, Yamamoto Yutaro, Katabami Takuyuki, Kurihara Isao, Saito Kohei, Kanamoto Naotetsu, Fukuoka Hidenori, Wada Norio, Murabe Hiroyuki, Inoue Tatsuhi |
KDM1A inactivation causes hereditary food-dependent Cushing syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 2021 12 24 (2): 374-383. Vaczlavik Anna, Bouys Lucas, Violon Florian, Giannone Gaetan, Jouinot Anne, Armignacco Roberta, Cavalcante Isadora P, Berthon Annabel, Letouzé Eric, Vaduva Patricia, Barat Maxime, Bonnet Fidéline, Perlemoine Karine, Ribes Christopher, Sibony Mathilde, North Marie-Odile, Espiard Stéphanie, Emy Philippe, Haissaguerre Magalie, Tauveron Igor, Guignat Laurence, Groussin Lionel, Dousset Bertrand, Reincke Martin, Fragoso Maria C, Stratakis Constantine A, Pasmant Eric, Libé Rossella, Assié Guillaume, Ragazzon Bruno, Bertherat Jérô |
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- Page last updated:Apr 22, 2024
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