Limb girdle muscular dystrophy 2A (HG-U133A) - - GEO DataSets

Warning: The NCBI web site requires JavaScript to function. more...

Result Filters

Summary

Format

Summary
Summary (text)
Unique Identifier List

Send to:

Choose Destination

File
Clipboard
Collections

Links from GEO Profiles

Limb girdle muscular dystrophy 2A (HG-U133A)

Analysis of skeletal muscles from patients with limb girdle muscular dystrophy 2A (LGMD2A). LGMD2A is a recessive genetic disorder caused by mutations in calpain 3 (CAPN3). Results provide insight into the molecular pathogenesis of LGMD2A.

Organism:: Homo sapiens

Type:: Expression profiling by array, transformed count, 2 disease state sets

Platform:: GPL96
Series:: GSE11681
20 Samples

Download data: CEL

DataSet

Accession:: GDS3474

ID:: 3474

PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet

Supplemental Content

Related information

PubMed
Related PubMed entries
Full text in PMC
PMC links
Similar studies
Similar studies
GEO Profiles
Related GEO
BioProject
BioProject links
GEO DataSets
Related GEO DataSets
Taxonomy
Taxonomy

Important Links

Recent activity

Clear Turn Off Turn On

Limb girdle muscular dystrophy 2A (HG-U133A)
Limb girdle muscular dystrophy 2A (HG-U133A)
Accession: GDS3474

GEO DataSets
Related DataSets for GEO Profiles (Select 57889479) (1)
GEO DataSets

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

You are here: NCBI > Genes & Expression > Gene Expression Omnibus (GEO) Datasets

Support Center

GEO DataSets

Functional Genomics Studies