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Items: 3

1.

Small RNA-seq analysis of circulating miRNAs to identify phenotypic variability in Friedreich's ataxia patients

(Submitter supplied) Friedreich’s ataxia (FRDA; OMIM 229300), an autosomal recessive neurodegenerative mitochondrial disease, is the most prevalent hereditary ataxia. In addition, FRDA patients showed additional non-neurological features such as scoliosis, diabetes and cardiac complications. Hypertrophic cardiomyopathy, which is found in two thirds of patients at the time of diagnosis, is the primary cause of death in these patients. more...
Organism:
Homo sapiens
Type:
Non-coding RNA profiling by high throughput sequencing
Platform:
GPL15456
42 Samples
Download data: TXT
Series
Accession:
GSE105052
ID:
200105052

PubMed Full text in PMC Similar studies SRA Run Selector

2.

Illumina HiScanSQ (Homo sapiens)

Organism:
Homo sapiens
122 Series
2006 Samples
Download data
Platform
Accession:
GPL15456
ID:
100015456

3.

Control_10

Organism:
Homo sapiens
Source name:
Plasma
Platform:
GPL15456
Series:
GSE105052
Download data
Sample
Accession:
GSM2817030
ID:
302817030

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db=gds|term=GSM2817030[Accession]|query=5|qty=2|blobid=MCID_673bb3f0a56b24050d385f2c|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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