Infantile-onset Pompe disease: biceps - - GEO DataSets - NCBI

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

Full record GDS4410

Infantile-onset Pompe disease: biceps

Analysis of biceps biopsies from untreated patients with infantile-onset Pompe. Pompe disease is a genetic disorder resulting from lysosomal acid alpha-glucosidase (GAA) deficiency; the severest form affects infants. Results provide insight into the molecular basis of infantile-onset Pompe disease.

Organism:: Homo sapiens

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

Platform:: GPL570
Series:: GSE38680
19 Samples

Download data: CEL

DataSet

Accession:: GDS4410

ID:: 4410

PubMed Similar studies GEO Profiles Analyze DataSet

Supplemental Content

Related information

PubMed
Related PubMed entries
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

Related DataSets for GEO Profiles (Select 89116219) (1)
GEO DataSets
Infantile-onset Pompe disease: biceps
Infantile-onset Pompe disease: biceps
Accession: GDS4410

GEO DataSets
Related DataSets for GEO Profiles (Select 89135097) (1)
GEO DataSets
Related DataSets for GEO Profiles (Select 89143794) (1)
GEO DataSets
Related DataSets for GEO Profiles (Select 89124597) (1)
GEO DataSets

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

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