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Full record GDS2175

Cockayne syndrome group B protein-null fibroblast rescue (HG-U133A)

Analysis of Cockayne syndrome group B (CSB) protein-null fibroblasts rescued by expression of CSB cDNA. CS, a neurodegenerative disorder, arises mostly from CSB defects. Results provide insight into how CSB defects cause CS.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 protocol sets
Platform:
GPL96
Series:
GSE3407
8 Samples
Download data: CEL

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