hereditary spastic paraplegia 2

Summary
Synonym
  • SPG2
  • X-linked spastic paraplegia 2
  • spastic paraplegia type 2
Definition
A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2.
Super Class
X-linked recessive disease hereditary spastic paraplegia
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5354 PLP1 proteolipid protein 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
18823 Plp1 proteolipid protein (myelin) 1

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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