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A point mutation in the nuclear speckle protein and splicing factor SRRM2 is associated with amyotrophic lateral sclerosis and causes dysregulation of synapse-associated genes

geo / GSE307674

Dataset

Provider: GEO
Type: bulk
Organism: Homo sapiens (tax 9606)
Format / file: counts_table — GSE307674_counts_SRRM2_S1444P.txt.gz (673 KB)
Matrix: 6 samples
Source page: https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE307674
Download URL: https://ftp.ncbi.nlm.nih.gov/geo/series/GSE307nnn/GSE307674/suppl/GSE307674_counts_SRRM2_S1444P.txt.gz

DOIs

None

PubMed IDs

Accessions

Not in ASAP yet.