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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Bibliographic Details
Main Authors: Michael Brockmann, Verena Schildgen, Oliver Schildgen, Jessica Lüsebrink, Monika Pieper, Alexandru Gudima
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Data in Brief
Online Access:http://www.sciencedirect.com/science/article/pii/S2352340918308564