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GSE27433
Genome-wide consequences of compromised NMD and their relavence for variable clinical phenotype of patients with UPF3B mutations
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Homo sapiens
18 Downloadable Samples
Affymetrix Human Exon 1.0 ST Array [transcript (gene) version (huex10st), Affymetrix Human Human Exon 1.0 ST Array (huex10st)
Submitter Supplied Information
Description
This SuperSeries is composed of the SubSeries listed below.
PubMed ID
22182939
Publication Title
Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability.
Total Samples
32
Submitter’s Institution
SA Pathology
Authors
Nguyen LS
,
Jolly L
,
Shoubridge C
,
Chan WK
,
Huang L
,
Laumonnier F
,
Raynaud M
,
Hackett A
,
Field M
,
Rodriguez J
,
Srivastava AK
,
Lee Y
,
Long R
,
Addington AM
,
Rapoport JL
,
Suren S
,
Hahn CN
,
Gamble J
,
Wilkinson MF
,
Corbett MA
,
Gecz J
Source Repository
Gene Expression Omnibus (GEO)
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