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

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https://hal.archives-ouvertes.fr/hal-02025621
Contributor : Laure-Hélène Davoine Connect in order to contact the contributor
Submitted on : Tuesday, February 19, 2019 - 5:20:50 PM
Last modification on : Tuesday, July 20, 2021 - 5:20:07 PM

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  • HAL Id : hal-02025621, version 1

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E. Panagiotakaki, E. de Grandis, M. Stagnaro, E. L. Heinzen, C. Fons, et al.. Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood-a study of 155 patients. Orphanet journal of rare diseases, 2015, 10, pp.123. ⟨hal-02025621⟩

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