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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 ofSMARCB1Deficiency

Journal Article published 2015 in BioMed Research International volume 2015 on pages 1 to 12

Research funded by Svenska Forskningsrådet Formas

Authors: Johanna Sandgren, Stefan Holm, Ana Maria Marino, Jurate Asmundsson, Pernilla Grillner, Monica Nistér, Teresita Díaz de Ståhl