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Multimodal electrophysiologic follow-up study in 3 mutated but presymptomatic members of a spinocerebellar ataxia type 1 (SCA1) family
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2005
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Follow-up StudyNeurological DisorderMedicineMotor DisorderNeuroscienceNeurologyCentral Nervous SystemNeuropathologyNeuromuscular PathologySynaptic SignalingPresymptomatic Members
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