GEO DataSets

(Submitter supplied) Spinal muscular atrophy (SMA) is an autosomal recessive, pediatric-onset disorder caused by the loss of spinal motor neurons thereby leading to generalized muscle atrophy. SMA is caused by the loss of or mutations in the survival motor neuron 1 (SMN1) gene. SMN1 is duplicated only in human to give rise to the paralogous SMN2 gene. These paralogs are nearly identical except for a cytosine to thymine (C-to-T) transition within an exonic splicing enhancer (ESE) element within exon 7. more...

Organism:

Homo sapiens

Type:

Expression profiling by array

Platform:

GPL23126

9 Samples

Download data: CEL

(Submitter supplied) Annotation was derived from the Affymetrix annotation file Clariom_D_Human.na36.hg38.transcript.csv: #%create_date=Mon Jun 20 14:19:01 2016 PDT #%chip_type=Clariom_D_Human #%lib_set_name=Clariom_D_Human #%lib_set_version=r1 #%genome-species=Homo sapiens #%genome-version=hg38 #%genome-version-ucsc=hg38 #%genome-version-ncbi=GRCh38 #%genome-version-create_date=2013-12-00 #%genome-lifted-method=psl-map.pl #%genome-lifted_from-species=Homo sapiens #%genome-lifted_from-version-ucsc=hg38 #%genome-lifted_from-version-ncbi=GRCh38 #%netaffx-annotation-date=2016-06-03 #%netaffx-annotation-netaffx-build=36 Protocol: See manufacturers website

Organism:

Homo sapiens

287 Series

2 Related Platforms

6219 Samples

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