Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients
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S. Tsuji | S. Morishita | H. Ishiura | J. Mitsui | H. Oguni | J. Yoshimura | M. Sasaki | S. Hirose | Yoshiaki Saito | A. Ishii | S. Kimura | H. Arai | S. Yamashita