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Acemap > Paper > Aprataxin遺伝子変異（689insT）が認められた眼球運動失行を伴う失調症（Ataxia-oculomotor apraxia; AOA1）患者の臨床症状

Aprataxin遺伝子変異（689insT）が認められた眼球運動失行を伴う失調症（Ataxia-oculomotor apraxia; AOA1）患者の臨床症状

2009 
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