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Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency

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第一作者： Johanna Sgren

作者： Johanna Sgren ^[1] ; Stefan Holm ; Ana Maria Marino ; Jurate Asmundsson ; Pernilla Grillner ; Monica Nister ; Teresita Diaz de Stahl

作者单位： Department of Oncology-Pathology, Karolinska Institutet ^[1]

发布时间 2020-12-17

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BioMed research international

2015年2015卷34期

ArticleID862039-ArticleID862039页

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BioMed research international

2015年2015卷34期

ArticleID862039-ArticleID862039页

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Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency

BioMed research international

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Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency

BioMed research international

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BioMed research international

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