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Whole exome- and mRNA-sequencing of an AT/RT case reveals few somatic mutations and several deregula...

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Whole exome- and mRNA-sequencing of an AT/RT case reveals few somatic mutations and several deregula...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A458163643

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

About this item

Full title

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

Author / Creator

Sandgren, Johanna , Holm, Stefan , Marino, Ana Maria , Asmundsson, Jurate , Grillner, Pernilla , Nister, Monica and de Stahl, Teresita Diaz

Publisher

John Wiley & Sons, Inc

Journal title

BioMed Research International, 2015

Language

English

Formats

Reports

Publication information

Publisher

John Wiley & Sons, Inc

Subjects

More information

Alternative Titles

Full title

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

Authors, Artists and Contributors

Author / Creator

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_gale_infotracmisc_A458163643

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A458163643

Other Identifiers

ISSN

2314-6133

DOI

10.1155/2015/862039

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