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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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LvYWangZLiuCCuiLIdentification of a novel CACNA1A mutation in a Chinese family with auto-somal recessive progressive myoclonic epilepsyNeuropsychiatr Dis Treat2017191326312636
Web of Science ®Google Scholar
ZhuchenkoOBaileyJBonnenPAutosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channelNat Genet199715162698988170
PubMed Web of Science ®Google Scholar

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