SPG23: Difference between revisions

SPG23
Identifiers
Aliases	SPG23, spastic paraplegia 23 (autosomal recessive)
External IDs	GeneCards: SPG23; OMA:SPG23 - orthologs
Orthologs
	353293
	n/a
	n/a
	n/a
	n; a
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	n/a
	n/a
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	Wikidata
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Revision as of 13:42, 11 August 2021

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]

^ "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.

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.

This article on a gene on human chromosome 1 is a stub. You can help Wikipedia by expanding it.

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-{{Underlinked|date=January 2021}}
 {{Infobox_gene}}
 '''Spastic paraplegia 23 (SPG [[Autosomal Recessive|autosomal recessive]])'''<ref name="entrez">{{cite web|url=https://www.ncbi.nlm.nih.gov/gene/353293|title=Entrez Gene: Spastic paraplegia 23 (autosomal recessive)}}</ref> is a 25cM [[Locus (genetics)|gene locus]] at 1q24-q32.<ref>{{Cite web|url=https://www.genenames.org/cgi-bin/gene_symbol_report?hgnc_id=HGNC:21340|title=SPG23 Symbol Report {{!}} HUGO Gene Nomenclature Committee|website=www.genenames.org|access-date=2017-09-29}}</ref> A [[Genetic linkage|genome-wide linkage]] screen has associated this locus with a type of [[hereditary spastic paraplegia]] (HSP).<ref>{{cite journal | vauthors = 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 | title = A locus for complicated hereditary spastic paraplegia maps to chromosome 1q24-q32 | journal = Annals of Neurology | volume = 54 | issue = 6 | pages = 796–803 | date = December 2003 | pmid = 14681889 | doi = 10.1002/ana.10768 | s2cid = 12631177 | url = https://www.ncbi.nlm.nih.gov/pubmed/?term=A+Locus+for+Complicated+Hereditary+Spastic+Paraplegia+Maps+to+Chromosome+1q24-q32 }}</ref>