BaseSpace
Correlation
Engine-Public
Sign In
Register
Correlation Engine 2.0
Home
My Data
Bookmarks
Collaborations
Inbox
Import Your Data
QuickView
FAQ
What is QuickView?
What can my QuickView results tell me?
What are the sources for the General Info tab in QuickView?
More QuickView FAQs
Back to top
QuickView
Curated
Studies
Body
Atlas
Disease
Atlas
Pharmaco
Atlas
Knockdown
Atlas
Genetic
Markers
Pathway
Enrichment
Literature
Clinical
Trials
0
Meta-
Analysis
QuickView
Search sequence regions
(e.g.
Acetaminophen
,
rs7903146
,
FXYD4
,
cell-cell adhesion
,
Influenza
,
Retina
,
Autoimmunity
)
Organisms
Chromosomes
Start
Stop
Homo Sapiens
Mus Musculus
Rattus Norvegicus
C. Elegans
D. Melanogaster
Saccharomyces Cerevisiae
QuickView
Go back to main search
Bookmark
Forward
QuickView
for
X-linked retinitis pigmentosa
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Retinal dystrophy
OMIM - Congenital disorder
OMIM - Multisystem Complex Disorders
OMIM - Intellectual Development Neurological and Behavioral Disorders
Explore Curated Studies Results
Literature
Most Relevant Literature
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a …
The X-linked retinitis pigmentosa protein RP2 facilitates G protein traffic.
Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked r…
Novel RPGR-ORF15 mutations in X-linked retinitis pigmentosa patients.
Structural and functional characteristics in carriers of X-linked retinitis pigmentosa with a tapeta…
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
Clinical Evaluation of Patients With X-linked Retinitis Pigmentosa (XLRP)
4D-125 in Patients With X-Linked Retinitis Pigmentosa (XLRP)
DHA and X-Linked Retinitis Pigmentosa
Natural History of the Progression of X-Linked Retinitis Pigmentosa
Gene Therapy for X-linked Retinitis Pigmentosa (XLRP) Retinitis Pigmentosa GTPase Regulator (RPGR)
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ