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Genetics of multiple endocrine neoplasia type 1 syndrome: what's new and what's old
Despite its identification in 1997, the functions of the MEN1 gene—the main gene underlying multiple endocrine neoplasia type 1 syndrome—are not yet fully understood. In addition, unlike the RET—MEN2 causative gene—no hot-spot mutational areas or genotype–phenotype correlations have been identified....
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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F1000Research
2017
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288685/ https://www.ncbi.nlm.nih.gov/pubmed/28184288 http://dx.doi.org/10.12688/f1000research.7230.1 |