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Items: 3

1.

OTX2 loss causes rod differentiation defect in CRX-associated congenital blindness

(Submitter supplied) Leber congenital amaurosis (LCA) includes congenital or early-onset blinding diseases, characterized by vision loss together with nystagmus and nonrecordable electroretinogram (ERG). At least 19 genes are associated with LCA. While most LCA is recessive, mutations in the homeodomain transcription factor gene CRX lead to autosomal dominant LCA. The mechanism of CRX-LCA is not understood. Here, we report a new spontaneous mouse mutant carrying a frameshift mutation in Crx (CrxRip). more...
Organism:
Mus musculus
Type:
Expression profiling by high throughput sequencing
Platform:
GPL11002
20 Samples
Download data: TXT
Series
Accession:
GSE52006
ID:
200052006
2.

Illumina Genome Analyzer IIx (Mus musculus)

Platform
Accession:
GPL11002
ID:
100011002
3.

P2_Hom_rep2

Organism:
Mus musculus
Source name:
CrxRip/Rip mouse retina at age postnatal day 2
Platform:
GPL11002
Series:
GSE52006
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Sample
Accession:
GSM1257269
ID:
301257269
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db=gds|term=GSM1257269[Accession]|query=1|qty=2|blobid=MCID_65d69750bf197b1b5ead9f05|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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