SPG9 explained
Spastic paraplegia 9 (autosomal dominant) is a protein that in humans is encoded by the SPG9 gene.[1]
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 . 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 . February 1999 . 9973297 . 1377769 . 10.1086/302241 .
Notes and References
- Web site: Entrez Gene: Spastic paraplegia 9 (autosomal dominant) .
