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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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| Vydáno v: | J Endocr Soc |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2020
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| Témata: | |
| On-line přístup: | 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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