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Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the ATP13A2 Gene.

Hussein AlgahtaniBader ShirahSalem AlshammariFareeda AlghamdiAngham Abdulrhman AbdulkareemMuhammad Imran Naseer
Published in: Movement disorders clinical practice (2022)
Keyphrases
  • cerebral palsy
  • copy number
  • genome wide
  • intellectual disability
  • botulinum toxin
  • genome wide identification
  • upper limb
  • muscular dystrophy
  • autism spectrum disorder
  • dna methylation
  • transcription factor