(Q32143030)

English

hereditary spastic paraplegia 43

hereditary spastic paraplegia that has material basis in mutation in the C19ORF12 gene on chromosome 19q12

  • SPG43
  • autosomal recessive spastic paraplegia type 43
  • autosomal recessive spastic paraplegia 43
  • hereditary spastic paraplegia type 43
  • SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE
  • SPASTIC PARAPLEGIA 43, AUTOSOMAL RECESSIVE; SPG43

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