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Published in 2022 at "International Journal of Molecular Sciences"
DOI: 10.3390/ijms23126874
Abstract: Mutations in the EPM2A gene encoding laforin cause Lafora disease (LD), a progressive myoclonic epilepsy characterized by drug-resistant seizures and progressive neurological impairment. To date, rodents are the only available models for studying LD; however,…
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Keywords:
trehalose treatment;
disease;
zebrafish model;
model ... See more keywords