Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype. (Q43999068)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype. |
scientific article |
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Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype (English)
Subramaniam Ganesh
Silvana Francheschetti
Concetta Riggio
Giuiliano Avanzini
Adrian Rabinowicz
Saeed Bohlega
Julia Bailey
Maria E Alonso
Astrid Rasmussen
Alfredo E Thomson
Adriana Ochoa
Aurelio J Prado
Marco T Medina
Kazuhiro Yamakawa