Biology:SPG9
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Revision as of 18:12, 1 May 2022 by imported>JOpenQuest (add)
Short description: Genetic element in the species Homo sapiens
 Generic protein structure example |
Spastic paraplegia 9 (autosomal dominant) is a protein that in humans is encoded by the SPG9 gene.[1]
References
Further reading
- "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. doi:10.1086/302241. PMID 9973297.
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