Biology:SPG23

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Short description: Genetic element in the species Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Spastic paraplegia 23 (SPG autosomal recessive)[1] is a 25cM gene locus at 1q24-q32.[2] A genome-wide linkage screen has associated this locus with a type of hereditary spastic paraplegia (HSP).[3]

References

  1. ↑ "Entrez Gene: Spastic paraplegia 23 (autosomal recessive)". https://www.ncbi.nlm.nih.gov/gene/353293. 
  2. ↑ "SPG23 Symbol Report | HUGO Gene Nomenclature Committee". https://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=HGNC:21340. 
  3. ↑ "A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32". Annals of Neurology 54 (6): 796–803. December 2003. doi:10.1002/ana.10768. PMID 14681889. 

Further reading

  • "A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32". Annals of Neurology 54 (6): 796–803. December 2003. doi:10.1002/ana.10768. PMID 14681889. 




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