Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations
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ABSTRACT: This SuperSeries is composed of the following subset Series: GSE27125: Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [mRNA profiling] GSE27199: Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [RNA-seq] GSE27412: Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations [CNV] Refer to individual Series
ORGANISM(S): Homo sapiens
SUBMITTER: Jozef Gecz
PROVIDER: E-GEOD-27433 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
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