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Full record GDS849

Hereditary spastic paraparesis

Analysis of gene expression in skeletal muscle of three patients affected by hereditary spastic paraplegia (HSP) caused by mutations of spastin (SPG4). SPG4 is an ubiquitously expressed protein involved in microtubule regulation and vesicle traffic.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 individual sets
Platform:
GPL8300
Series:
GSE1300
3 Samples
Download data: CEL
DataSet
Accession:
GDS849
ID:
849

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