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

<div>Fraction of expressed/not expressed uncommon and damaging germline variants.</div>

BioMed Research International

fig3

Figure 3

Figure 3: Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of <i>SMARCB1</i> Deficiency 

Figure 3 | 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 