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for
axonal neuropathy
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
COA7
GAN
NEMF
HINT1
DCAF8
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
cullin-RING ubiquitin ligase complex
GSE3982_NKCELL_VS_TH2_DN
GSE14769_UNSTIM_VS_120MIN_LPS_BMDM_UP
GSE32986_GMCSF_AND_CURDLAN_LOWDOSE_VS_GMCSF_AND_CURDLAN_HIGHDOSE_STIM_DC_UP
ubiquitin ligase complex
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Curated Studies
Most Correlated Studies
Mouse Phenotypes - Disorder of head
OMIM - Neuropathy
OMIM - Intellectual Development Neurological and Behavioral Disorders
OMIM - Spinocerebellar Ataxias
OMIM - Neuromyotonia
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Literature
Most Relevant Literature
Involvement of the globus pallidus in giant axonal neuropathy.
Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion a…
Clinical and genetic studies in a Chinese family with giant axonal neuropathy.
Motor Axonal Neuropathy Associated With Idiopathic CD4(+) T-Lymphocytopenia.
Giant axonal neuropathy caused by a novel compound heterozygous mutation in the gigaxonin gene.
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Clinical Trials
Most Relevant Clinical Trials
Giant Axonal Neuropathy Natural History Study
Intrathecal Administration of scAAV9/JeT-GAN for the Treatment of Giant Axonal Neuropathy
Use of QTRAC Technique to Measure Axonal Excitability in Anti-MAG Neuropathy
Axon Therapy and Conventional Medical Management for Painful Diabetic Neuropathy Compared to Sham an…
Pain In Neuropathy Study
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