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MON-509 RET Mutations in the MEN1 Syndrome: Is It an Innocent Bystander?
Introduction MENIN and RET mutations in MEN1 families, are rare, and, when they co-exist either mutation may predominate the clinical picture. We report a family, with both mutations, and, suspect that the RET mutation may not be an innocent bystander. Clinical Cases GM (36M): 2009: Presented with s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207450/ http://dx.doi.org/10.1210/jendso/bvaa046.1622 |