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Segregation of ATP10B variants in families with autosomal recessive parkinsonism.

Christelle TessonEbba LohmannDavid DevosHélène BertrandSuzanne LesageAlexis Brice
Published in: Acta neuropathologica (2020)
Keyphrases
  • copy number
  • parkinson disease
  • intellectual disability
  • drug induced
  • muscular dystrophy
  • autism spectrum disorder
  • deep brain stimulation
  • dna methylation
  • genome wide
  • duchenne muscular dystrophy