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Article Source: Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients
Ishii A, Saito Y, Mitsui J, Ishiura H, Yoshimura J, et al. (2013) Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients. PLoS ONE 8(2): e56120. doi: 10.1371/journal.pone.0056120

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