학술논문
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
Document Type
Article
Author
Source
In: BioMed Research International . (BioMed Research International, 2015, 2015)
Subject
Language
English
ISSN
23146141
23146133
23146133