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Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients
- Atsushi Ishii,
- Yoshiaki Saito,
- Jun Mitsui,
- Hiroyuki Ishiura,
- Jun Yoshimura,
- Hidee Arai,
- Sumimasa Yamashita,
- Sadami Kimura,
- Hirokazu Oguni,
- Shinichi Morishita
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- Published: February 8, 2013
- https://doi.org/10.1371/journal.pone.0056120
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