Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients.
| Autor: | Panagiotakaki, Eleni1 eleni.panagiotakaki@chu-lyon.fr, De Grandis, Elisa2, Stagnaro, Michela2, Heinzen, Erin L.3,4, Fons, Carmen5, Sisodiya, Sanjay6, de Vries, Boukje7, Goubau, Christophe8, Weckhuysen, Sarah9, Kemlink, David10, Scheffer, Ingrid11,12, Lesca, Gaëtan13,14, Rabilloud, Muriel15, Klich, Amna15, Ramirez-Camacho, Alia1,5, Ulate-Campos, Adriana5, Campistol, Jaume5, Giannotta, Melania16, Moutard, Marie-Laure17, Doummar, Diane17 |
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| Zdroj: | Orphanet Journal of Rare Diseases. 9/27/2015, Vol. 10 Issue 1, p1-13. 13p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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