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NGS-dataset of putative driver mutations associated with benign peritoneal strumosis

A rare case of benign peritoneal strumosis was screened for driver mutations in genes relevant to currently approved cancer therapies. Therefore, three formalin fixed paraffin embedded issue sections were screened with the GeneReader Actionable Insights NGS panel (Qiagen, Hilden, Germany) for the oc...

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Detalles Bibliográficos
Publicado en:Data Brief
Main Authors: Brockmann, Michael, Schildgen, Verena, Schildgen, Oliver, Lüsebrink, Jessica, Pieper, Monika, Gudima, Alexandru
Formato: Artigo
Idioma:Inglês
Publicado: Elsevier 2018
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6122335/
https://ncbi.nlm.nih.gov/pubmed/30186896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dib.2018.08.006
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