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

Author(s):
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 (0000-0002-9310-5535); Mikati, M.; Goldstein, D.B.; Vavassori, R.; Arzimanoglou, A.; IBAHC Consortium; French AHC Consortium; Int AHC Consortium
Published
2015
Publication type
Article / Letter to editor
Alternating hemiplegia of childhoodATP1A3Genotype-phenotype
Date issued
2015-09-26
Language
English
Is part of
Orphanet Journal of Rare Diseases
hdl
1887/105426
doi
10.1186/s13023-015-0335-5