(Q32143203)

English

hereditary spastic paraplegia 56

hereditary spastic paraplegia that has material basis in mutation in the CYP2U1 gene on chromosome 4q25

  • SPG56
  • autosomal recessive spastic paraplegia type 56
  • autosomal recessive spastic paraplegia 56
  • SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE
  • SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE; SPG56
  • hereditary spastic paraplegia type 56

Statements

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C190870
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Identifiers

 
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