OR06-01 The Role of Germline Defects in Cushing’s Disease

J.L.M. and C.A.S. contributed equally. Introduction: Cushing’s Disease (CD) has been described as a component of a number of familial genetic syndromes. Yet, such cases may go largely unrecognized due to phenotypic variability, incomplete penetrance, and the rarity of the disease. We determined the...

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Publicat a:J Endocr Soc
Autors principals: Hernández-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Faucz, Fabio R, Chittiboina, Prashant, Denise, Kay M, Mills, James L, Stratakis, Constantine A
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
Matèries:
Neuroendocrinology and Pituitary
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7209272/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.323
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