SPG9
| 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
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Spastic paraplegia 9 (autosomal dominant)".
Further reading
- 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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