DOI: 10.1055/s-00000071

Seminars in Neurology

References

Koskenkorva P, Hyppönen J, Aikiä M , et al.
Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB gene.

Neurodegener Dis 2011;
8 (6) 515-522

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