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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...
Autores principales: | Jyotsna, Viveka P., Malik, Ekta, Birla, Shweta, Sharma, Arundhati |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549893/ https://www.ncbi.nlm.nih.gov/pubmed/26307114 http://dx.doi.org/10.1186/s12902-015-0041-2 |
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