SPG23

SPG23
Identifiers
Aliases	SPG23, spastic paraplegia 23 (autosomal recessive)
External IDs	GeneCards: SPG23
Orthologs
	353293
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	n; a
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	Wikidata
View/Edit Human

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[edit]

^ "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. Archived from the original on 2017-09-29. 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.

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.

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