Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations

✍ Scribed by Canafoglia, Laura; Gennaro, Elena; Capovilla, Giuseppe; Gobbi, Giuseppe; Boni, Antonella; Beccaria, Francesca; Viri, Maurizio; Michelucci, Roberto; Agazzi, Pamela; Assereto, Stefania; Coviello, Domenico A.; Di Stefano, Maria; Rossi Sebastiano, Davide; Franceschetti, Silvana; Zara, Federico

• Book ID: 119855226
• Publisher: Wiley (Blackwell Publishing)
• Year: 2012
• Tongue: English
• Weight: 592 KB
• Volume: 53
• Category: Article
• ISSN: 0013-9580
• DOI: 10.1111/j.1528-1167.2012.03718.x