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Canafoglia L, Gennaro E, Capovilla G, Gobbi G, Boni A, Beccaria F, Viri M, Michelucci R, Agazzi P, Assereto S, Coviello DA, Di Stefano M, Rossi Sebastiano D, Franceschetti S, Zara F. (2012) Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations. Epilepsia 53:2120–2127.

The errors in the above article pertain to the reported mutations. Specifically, they are:

  1. In the paper we described the same mutation as c.168+2_169+21delinsAA (in the text) or c.168+2-168+21delinsAA (in the table). The author confirms that the mutation is c.168+2_168+21delinsAA
  2. The reported mutation: c.133C>T is wrong. The author confirms that the mutation is c.136C>T.