| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Lafora progressive myoclonus epilepsy: a meta-analysis of reported mutations in the first decade following the discovery of the EPM2A and NHLRC1 genes. | Hum Mutat | 2009 | 1.02 |
| 2 | Mutations in the NHLRC1 gene are the common cause for Lafora disease in the Japanese population. | J Hum Genet | 2005 | 0.88 |
| 3 | Lafora disease in the Indian population: EPM2A and NHLRC1 gene mutations and their impact on subcellular localization of laforin and malin. | Hum Mutat | 2008 | 0.88 |