SPG9

SPG9
Identifiers
Aliases	SPG9, spastic paraplegia 9 (autosomal dominant)
External IDs	GeneCards: SPG9; OMA:SPG9 - orthologs
Orthologs
	9193
	n/a
	n/a
	n/a
	n; a
	n/a
	n/a
	n/a
	n/a
	n/a
	Wikidata
View/Edit Human

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)".

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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