U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

Links from GEO Profiles

Full record GDS2613

Rett syndrome: brain frontal cortex

Analysis of brain frontal cortices of individuals with Rett syndrome (RTT). RTT is an X-linked neurodevelopmental disorder linked to heterozygous de novo mutations in MECP2, a gene encoding methyl-CpG-binding protein 2. Results provide insight into molecular pathogenesis of RTT.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 disease state sets
Platform:
GPL8300
Series:
GSE6955
6 Samples
Download data: CEL, EXP
DataSet
Accession:
GDS2613
ID:
2613

PubMed Similar studies GEO Profiles Analyze DataSet

Supplemental Content

Related information

Important Links

Recent activity

Clear Turn Off Turn On

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
Support Center