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Genetic test in multiple endocrine neoplasia type 1 syndrome: An evolving story
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited tumour syndrome expressing various endocrine and non-endocrine lesions and tumours. Since the identification of the causative gene, the oncosuppressor gene MEN1, in 1997, genetic testing has revealed an important approach...
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| Publicado no: | World J Exp Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Inc
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4436936/ https://ncbi.nlm.nih.gov/pubmed/25992327 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5493/wjem.v5.i2.124 |
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