Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients

Panagiotakaki, E.; Grandis, E. de; Stagnaro, M.; Heinzen, E.L.; Fons, C.; Sisodiya, S.; ... ; Int AHC Consortium (2015)

Article / Letter to editor

• Alternating hemiplegia of childhood
• ATP1A3
• Genotype-phenotype

• All authors: Panagiotakaki, E.; Grandis, E. de; Stagnaro, M.; Heinzen, E.L.; Fons, C.; Sisodiya, S.; Vries, B. de; Goubau, C.; Weckhuysen, S.; Kemlink, D.; Scheffer, I.; Lesca, G.; Rabilloud, M.; Klich, A.; Ramirez-Camacho, A.; Ulate-Campos, A.; Campistol, J.; Giannotta, M.; Moutard, M.L.; Doummar, D.; Hubsch-Bonneaud, C.; Jaffer, F.; Cross, H.; Gurrieri, F.; Tiziano, D.; Nevsimalova, S.; Nicole, S.; Neville, B.; Maagdenberg, A.M.J.M. van den; Mikati, M.; Goldstein, D.B.; Vavassori, R.; Arzimanoglou, A.; IBAHC Consortium; French AHC Consortium; Int AHC Consortium
• Date: 2015-09-26
• Journal: Orphanet Journal of Rare Diseases
• Volume: 10
• DOI: doi:10.1186/s13023-015-0335-5