Myotonic dystrophy type 2: vastus lateralis biopsies - - GEO DataSets - NCBI

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Full record GDS5276

Myotonic dystrophy type 2: vastus lateralis biopsies

Analysis of vastus lateralis biopsies from myotonic dystrophy type 2 (DM2) patients. DM2 is a multisystemic disorder caused by a (CCTG)n repeat expansion in intron 1 of cellular nucleic acid-binding protein. Results provide insight into molecular mechanisms underlying DM2 pathogenesis.

Organism:: Homo sapiens

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

Platform:: GPL6102
Series:: GSE45331
10 Samples

DataSet

Accession:: GDS5276

ID:: 5276

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Myotonic dystrophy type 2: vastus lateralis biopsies
Myotonic dystrophy type 2: vastus lateralis biopsies
Accession: GDS5276

GEO DataSets
Related DataSets for GEO Profiles (Select 120292445) (1)
GEO DataSets
PMC Links for Gene (Select 9855) (38)
PMC
603029095F1 NIH_MGC_114 Homo sapiens cDNA clone IMAGE:5199551 5', mRNA sequence
603029095F1 NIH_MGC_114 Homo sapiens cDNA clone IMAGE:5199551 5', mRNA sequence
gi|15748478|gnl|dbEST|9597694|gb|BI 0.1|

Nucleotide
PREDICTED: Homo sapiens FERM, ARH/RhoGEF and pleckstrin domain protein 2 (FARP2)...
PREDICTED: Homo sapiens FERM, ARH/RhoGEF and pleckstrin domain protein 2 (FARP2), transcript variant X8, mRNA
gi|2217332468|ref|XM_011512236.2|

Nucleotide

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