SPG9: Difference between revisions
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Importing Wikidata short description: "Genetic element in the species Homo sapiens" (Shortdesc helper) |
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{{Short description|Genetic element in the species Homo sapiens}} |
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'''Spastic paraplegia 9 (autosomal dominant)''' is a [[protein]] that in humans is encoded by the SPG9 [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Spastic paraplegia 9 (autosomal dominant) | url = https://www.ncbi.nlm.nih.gov/gene/9193 }}</ref> |
'''Spastic paraplegia 9 (autosomal dominant)''' is a [[protein]] that in humans is encoded by the SPG9 [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: Spastic paraplegia 9 (autosomal dominant) | url = https://www.ncbi.nlm.nih.gov/gene/9193 }}</ref> |
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Latest revision as of 06:36, 27 March 2022
| SPG9 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | SPG9, spastic paraplegia 9 (autosomal dominant) | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: SPG9 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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| Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Spastic paraplegia 9 (autosomal dominant) is a protein that in humans is encoded by the SPG9 gene.[2]
References[edit]
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Spastic paraplegia 9 (autosomal dominant)".
Further reading[edit]
- Seri M, Cusano R, Forabosco P, Cinti R, Caroli F, Picco P, Bini R, Morra VB, De Michele G, Lerone M, Silengo M, Pela I, Borrone C, Romeo G, Devoto M (February 1999). "Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy". American Journal of Human Genetics. 64 (2): 586–93. doi:10.1086/302241. PMC 1377769. PMID 9973297.
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