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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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| Publicat a: | Data Brief |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Elsevier
2018
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| Matèries: | |
| Accés en línia: | 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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