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Germ-line mutations in p27(Kip1) cause a multiple endocrine neoplasia syndrome in rats and humans
MENX is a recessive multiple endocrine neoplasia-like syndrome in the rat. The tumor spectrum in MENX overlaps those of human multiple endocrine neoplasia (MEN) types 1 and 2. We mapped the MenX locus to the distal part of rat chromosome 4, excluding the homologs of the genes responsible for the MEN...
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| 主要な著者: | , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
2006
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1622862/ https://ncbi.nlm.nih.gov/pubmed/17030811 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0603877103 |
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