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Neuropsychiatric Disease and Treatment Volume 14, 2018 - Issue
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Letter

Response to the paper titled “Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy”

Tracey D GravesDepartment of Neurology, North West Anglia NHS Foundation Trust, Hinchingbrooke Hospital, Huntingdon, UK, [email protected]Correspondence[email protected]
Page 2329 | Published online: 11 Sep 2018

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