hereditary spastic paraplegia 49

Summary
Synonym
  • SPG49
  • autosomal recessive spastic paraplegia 49
  • autosomal recessive spastic paraplegia type 49
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32.
Super Class
autosomal recessive disease hereditary spastic paraplegia

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024