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MEN1 gene mutation with parathyroid carcinoma: first report of a familial case
BACKGROUND: The occurrence of parathyroid carcinoma in multiple endocrine neoplasia type I (MENI) is rare and the 15 cases of malignant parathyroid tumor reported so far have been associated with MENI in individuals and not with multiple members within a family. METHODS: We report on a 61-year-old m...
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| Publicado no: | Endocr Connect |
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| Main Authors: | , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bioscientifica Ltd
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5704445/ https://ncbi.nlm.nih.gov/pubmed/29097378 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EC-17-0207 |
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