DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Canafoglia L, Gennaro E, Capovilla G , et al.
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
Epilepsia 2012;
53 (12) 2120-2127
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