From Wikipedia, the free encyclopedia
Spastic paraplegia 23 (SPG autosomal recessive)[2] is a 25cM gene locus at 1q24-q32.[3] A genome-wide linkage screen has associated this locus with a type of hereditary spastic paraplegia (HSP).[4]
References[]
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Spastic paraplegia 23 (autosomal recessive)".
- ^ "SPG23 Symbol Report | HUGO Gene Nomenclature Committee". www.genenames.org. Retrieved 2017-09-29.
- ^ Blumen SC, Bevan S, Abu-Mouch S, Negus D, Kahana M, Inzelberg R, Mazarib A, Mahamid A, Carasso RL, Slor H, Withers D, Nisipeanu P, Navon R, Reid E (December 2003). "A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32". Annals of Neurology. 54 (6): 796–803. doi:10.1002/ana.10768. PMID 14681889. S2CID 12631177.
Further reading[]
- Blumen SC, Bevan S, Abu-Mouch S, Negus D, Kahana M, Inzelberg R, Mazarib A, Mahamid A, Carasso RL, Slor H, Withers D, Nisipeanu P, Navon R, Reid E (December 2003). "A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32". Annals of Neurology. 54 (6): 796–803. doi:10.1002/ana.10768. PMID 14681889. S2CID 12631177.
Categories:
- Genes on human chromosome
- Proteins
- Human chromosome 1 gene stubs