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PEX10-related autosomal recessive cerebellar ataxia with hearing loss.

Gül Demet Kaya ÖzçoraSatoko MiyatakeNaomichi MatsumotoMehmet CanpolatMurat ErdoğanRuslan BayramovSefer Kumandaş
Published in: Acta neurologica Belgica (2018)
Keyphrases
  • hearing loss
  • intellectual disability
  • early onset
  • muscular dystrophy
  • autism spectrum disorder
  • drug induced