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The Inherited p53 Mutation in the Brazilian Population
A common criticism of studying rare diseases is the often-limited relevance of the findings to human health. Here, we review ∼15 years of research into an unusual germline TP53 mutation (p.R337H) that began with its detection in children with adrenocortical carcinoma (ACC), a remarkably rare childho...
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| Izdano u: | Cold Spring Harb Perspect Med |
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| Glavni autori: | , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Cold Spring Harbor Laboratory Press
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5131754/ https://ncbi.nlm.nih.gov/pubmed/27663983 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a026195 |
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