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Global gene expression in neuroendocrine tumors from patients with the MEN1 syndrome
BACKGROUND: Multiple Endocrine Neoplasia type 1 (MEN1, OMIM 131100) is an autosomal dominant disorder characterized by endocrine tumors of the parathyroids, pancreatic islets and pituitary. The disease is caused by the functional loss of the tumor suppressor protein menin, coded by the MEN1 gene. Th...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC549185/ https://ncbi.nlm.nih.gov/pubmed/15691381 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1476-4598-4-9 |
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