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MON-335 Phenocopy of Multiple Endocrine Neoplasia Type 1 (MEN1) Due to a Germline Cell Division Cycle 73 (CDC73) Variant

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the combined occurrence of parathyroid tumors, and neuroendocrine tumors (NETs) of the pituitary and pancreas. MEN1 is caused by germline mutations of the tumor suppressor gene MEN1, which are found in >...

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Detalles Bibliográficos
Publicado en:J Endocr Soc
Main Authors: Lines, Kate, Nachtigall, Lisa, Dichtel, Laura, Cranston, Treena, Khairi, Shafaq, Boon, Hannah, Abedi, Parisa, Zhang, Xun, Kooblall, Kreepa, Stevenson, Mark, Klibanski, Anne, Thakker, Rajesh
Formato: Artigo
Idioma:Inglês
Publicado: Endocrine Society 2019
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6550911/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/js.2019-MON-335
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