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CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype

Authors

  1. Correspondence to Dr Jeffrey Lambe, Department of Neurology, St James’s Hospital, Dublin 8, Ireland; jeffrey.lambe{at}ucdconnect.ie
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Citation

Lambe J, Monaghan B, Munteanu T, et al
CAPN1 mutations broadening the hereditary spastic paraplegia/spinocerebellar ataxia phenotype

Publication history

  • Accepted March 14, 2018
  • First published April 20, 2018.
Online issue publication 
January 18, 2019

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