Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients (Q34586667)
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English | Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients |
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Identification of ATP1A3 mutations by exome sequencing as the cause of alternating hemiplegia of childhood in Japanese patients (English)
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Atsushi Ishii
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Yoshiaki Saito
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Jun Mitsui
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Hiroyuki Ishiura
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Jun Yoshimura
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Hidee Arai
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Sumimasa Yamashita
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Sadami Kimura
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Hirokazu Oguni
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Shinichi Morishita
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Shoji Tsuji
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Masayuki Sasaki
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Shinichi Hirose
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8 February 2013
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e56120
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8 February 2013
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