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Wikipedia

SPG23

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]

SPG23
Identifiers
AliasesSPG23, spastic paraplegia 23 (autosomal recessive)
External IDsGeneCards: SPG23
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed search[1]n/a
Wikidata
View/Edit Human

References edit

  1. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  2. ^ "Entrez Gene: Spastic paraplegia 23 (autosomal recessive)".
  3. ^ . www.genenames.org. Archived from the original on 2017-09-29. Retrieved 2017-09-29.
  4. ^ 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 edit

  • 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.


spg23, spastic, paraplegia, autosomal, recessive, 25cm, gene, locus, 1q24, genome, wide, linkage, screen, associated, this, locus, with, type, hereditary, spastic, paraplegia, identifiersaliases, spastic, paraplegia, autosomal, recessive, external, idsgenecard. 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 SPG23IdentifiersAliasesSPG23 spastic paraplegia 23 autosomal recessive External IDsGeneCards SPG23OrthologsSpeciesHumanMouseEntrez353293n aEnsembln an aUniProtnan aRefSeq mRNA n an aRefSeq protein n an aLocation UCSC n an aPubMed search 1 n aWikidataView Edit HumanReferences 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 Further reading editBlumen 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 nbsp This article on a gene on human chromosome 1 is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title SPG23 amp oldid 1212925200, wikipedia, wiki, book, books, library,

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