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Lafora disease
(phenotype)
Summary
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Genetic Markers
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NHLRC1
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
energy reserve metabolic process
polysaccharide metabolic process
energy derivation by oxidation of organic compounds
GSE4811_CLASSSICALY_ACTIVATED_VS_TYPE_2_ACTIVATED_MACROPHAGE_UP
autophagy
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OMIM - Epilepsy disorders
Mouse Phenotypes - Epilepsy
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Most Relevant Literature
Deciphering the Polyglucosan Accumulation Present in Lafora Disease Using an Astrocytic Cellular Mod…
Role of Astrocytes in the Pathophysiology of Lafora Disease and Other Glycogen Storage Disorders.
Trehalose Treatment in Zebrafish Model of Lafora Disease.
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease …
Lafora disease in a Beagle - diagnosis and therapy].
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Ketogenic Diet in Lafora Disease
Natural History and Functional Status Study of Patients With Lafora Disease
Clinical and Genetic Studies of Familial Presenile Dementia With Neuronal Inclusion Bodies
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