Associated Papers
Case report of Lafora disease: a rare genetic disorder manifesting as progressive myoclonic epilepsy.
Naderian R et al.
Bmc Neurology, 2025
Prognostic value of pathogenic variants in Lafora Disease: systematic review and meta-analysis of patient-level data.
Pondrelli F et al.
Orphanet Journal of Rare Diseases, 2023
37658439 (PubMed )
Supplement: 13023_2023_2880_MOESM2_ESM.xlsx › STAB1_EPM2A
Late onset Lafora disease and novel EPM2A mutations: breaking paradigms.
Jara-Prado A et al.
Epilepsy Research, 2014
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