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Full record GDS4526

Wfs1 deficiency model of Wolfram syndrome: hypothalamus

Analysis of hypothalami from Wfs1-knockout, 129SV animals. Wfs1 deletion models Wolfram syndrome (WS), an autosomal recessive disorder characterized by multiple endocrine failure. Results provide insight into the molecular mechanisms underlying WS.
Organism:
Mus musculus
Type:
Expression profiling by array, transformed count, 2 genotype/variation sets
Platform:
GPL6246
Series:
GSE33372
18 Samples
Download data: CEL
DataSet
Accession:
GDS4526
ID:
4526

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