DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Lesca G, Boutry-Kryza N, de Toffol B , et al.
Novel mutations in EPM2A and NHLRC1 widen the spectrum of Lafora disease.
Epilepsia 2010;
51 (9) 1691-1698
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