(Q32143385)

English

autosomal recessive spastic paraplegia type 76

hereditary spastic paraplegia that has material basis in mutation in the CAPN1 gene on chromosome 11q13

  • autosomal recessive spastic paraplegia 76
  • SPG76
  • hereditary spastic paraplegia 76
  • Spastic Paraplegia 76, Autosomal Recessive
  • hereditary spastic paraplegia type 76
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