SPG9
{{Short description|Genetic element in the species Homo sapiens}}
{{Infobox_gene}}
Spastic paraplegia 9 (autosomal dominant) is a protein that in humans is encoded by the SPG9 gene.{{cite web | title = Entrez Gene: Spastic paraplegia 9 (autosomal dominant) | url = https://www.ncbi.nlm.nih.gov/gene/9193 }}
References
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Further reading
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- {{cite journal | vauthors = 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 | title = 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 | journal = American Journal of Human Genetics | volume = 64 | issue = 2 | pages = 586–93 | date = February 1999 | pmid = 9973297 | pmc = 1377769 | doi = 10.1086/302241 }}
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