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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Cold Spring Harb Perspect Med
मुख्य लेखकों: Achatz, Maria Isabel, Zambetti, Gerard P.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Cold Spring Harbor Laboratory Press 2016
विषय:
ऑनलाइन पहुंच: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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