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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Detalles Bibliográficos
Autores principales: Jyotsna, Viveka P., Malik, Ekta, Birla, Shweta, Sharma, Arundhati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
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

Internet

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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