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.
calcium channel activity
,
Ischemia
,
Neuron
,
Hematopoietic cell
,
Tamoxifen
,
rs3825942
)
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
merosin
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Heart atrium
Heart ventricle
Pericardium
Omental adipose tissue
Synovial membrane
Explore Body Atlas Results
Disease Atlas
Most Correlated Diseases
Muscular dystrophy
Myopathy
Viral enteritis
Duchenne muscular dystrophy
Transplanted organ rejection
Explore Disease Atlas Results
Pharmaco Atlas
Most Correlated Compounds
lupeol
ponasterone A
degrasyn
Cefazolin
Antibodies, Anti-DNA
Explore Pharmaco Atlas Results
Knockdown Atlas
Most Correlated Gene Perturbations
Mir181a-2
SP5
PERP
MAMLD1
ELF5
Explore Knockdown Atlas Results
Curated Studies
Most Correlated Studies
Loading...
Explore Curated Studies Results
Literature
Most Relevant Literature
Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosi…
Peripheral nerve injury in LAMA2-related congenital muscular dystrophy patients].
Merosin-deficient congenital muscular dystrophy: A novel homozygous mutation in the laminin-2 gene.
LAMA2-related congenital muscular dystrophy complicated by West syndrome.
Atypical phenotype in two patients with LAMA2 mutations.
Explore Literature Results
Clinical Trials
Most Relevant Clinical Trials
LAMA2-related Muscular Dystrophy Brain Study
Retrospective Natural History Study of Infants and Toddlers With LAMA2-CMD
Fat and Glucose Metabolism in Fed and Fasted State in Patients With Low Skeletal Muscle Mass
The Natural History of Patients With Mutations in SEPN1 (SELENON) or LAMA2
Congenital Muscle Disease Study of Patient and Family Reported Medical Information
Explore Clinical Trials Results
search
→
result
search
→
result
See more about this page
See complete FAQ