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Items: 3

1.

Study of variants associated with Fuchs corneal endothelial dystrophy cases without expansion of CTG18.1 repeats

(Submitter supplied) Fuchs' endothelial corneal dystrophy (FECD) is an inherited bilateral eye disease associated with a reduction in the density and functionality of the corneal endothelium. FECD is a genetic disease with autosomal-dominant inheritance. Genetic variants in the TCF4 gene have the most direct association with sporadic late-onset FECD in Caucasian patients. Association of the intronic single-nucleotide polymorphism (SNP) rs613872 in TCF4 gene with FECD was discovered in the Genome-Wide Association Study (GWAS) performed by Baratz et al. more...
Organism:
Homo sapiens
Type:
Genome variation profiling by SNP array
Platform:
GPL32909
31 Samples
Download data: TAB
Series
Accession:
GSE219272
ID:
200219272

2.

InfiniumOmni2-5-8v1-5_A1

(Submitter supplied) See manufacturer's website
Organism:
Homo sapiens
1 Series
31 Samples
Download data
Platform
Accession:
GPL32909
ID:
100032909

3.

Dfu_228: blood_FECD_noexp_24

Organism:
Homo sapiens
Source name:
whole blood DNA
Platform:
GPL32909
Series:
GSE219272
Download data
Sample
Accession:
GSM6781658
ID:
306781658

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db=gds|term=GSM6781658[Accession]|query=1|qty=2|blobid=MCID_66ebb81fb3438a0576f88ec9|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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