Distinct neurological disorders with ATP1A3 mutations

✍ Scribed by Heinzen, Erin L; Arzimanoglou, Alexis; Brashear, Allison; Clapcote, Steven J; Gurrieri, Fiorella; Goldstein, David B; Jóhannesson, Sigurður H; Mikati, Mohamad A; Neville, Brian; Nicole, Sophie; Ozelius, Laurie J; Poulsen, Hanne; Schyns, Tsveta; Sweadner, Kathleen J; van den Maagdenberg, Arn; Vilsen, Bente

• Book ID: 122315922
• Publisher: The Lancet
• Year: 2014
• Tongue: English
• Weight: 991 KB
• Volume: 13
• Category: Article
• ISSN: 1474-4465
• DOI: 10.1016/S1474-4422(14)70011-0