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Novel MEN 1 gene findings in rare sporadic insulinoma—a case control study
BACKGROUND: Insulinomas, which are rare tumors causing hyperinsulinemic hypoglycemia are usually sporadic but may also occur in association with multiple endocrine neoplasia type 1 (MEN-1) syndrome an autosomal dominant disorder caused by MEN1 gene mutations. MEN1 encodes a nuclear protein Menin, a...
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| Publicado no: | BMC Endocr Disord |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4549893/ https://ncbi.nlm.nih.gov/pubmed/26307114 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12902-015-0041-2 |
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