Multiple Endocrine Neoplasia Type 1 (MEN1) Phenocopy Due to a Cell Cycle Division 73 (CDC73) Variant

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the combined occurrence of parathyroid tumors, pituitary adenomas, and pancreatic neuroendocrine neoplasms (PNENs). MEN1 is caused by germline MEN1 mutations in > 75% of patients, and the remaining 25% o...

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Dades bibliogràfiques
Publicat a:J Endocr Soc
Autors principals: Lines, Kate E, Nachtigall, Lisa B, Dichtel, Laura E, Cranston, Treena, Boon, Hannah, Zhang, Xun, Kooblall, Kreepa G, Stevenson, Mark, Thakker, Rajesh V
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2020
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7594654/
https://ncbi.nlm.nih.gov/pubmed/33150274
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa142
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