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Results 1 - 7 of 7 for Hereditary spastic paraplegia 15
  1. SPG11 gene 
    ... mutations are common in familial cases of complicated hereditary spastic paraplegia. Neurology. 2008 Apr 15;70(16 Pt 2):1384-9. doi: 10. ... H. Clinical heterogeneity and genotype-phenotype correlations in hereditary ... (SPG11). Eur J Neurol. 2008 Oct;15(10):1065-70. doi: 10.1111/j.1468- ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  2. TUBB4A gene 
    ... TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia. Mov Disord. 2015 May;30(6):854-8. doi: 10.1002/mds.26196. Epub 2015 Mar 15. Citation on PubMed Lohmann K, Wilcox RA, Winkler ...
    https://medlineplus.gov/genetics/gene/tubb4a - Genetics
  3. SPART gene 
    ... Brown NA, Crosby AH. Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons. Exp Cell Res. 2006 Sep 10;312(15):2764-77. doi: 10.1016/j.yexcr.2006. ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  4. WASHC5 gene 
    ... 1 syntrophin. Am J Med Genet. 2000 May 15;92(2):122-7. doi: ... locus cause hereditary spastic paraplegia. Am J Hum Genet. 2007 Jan;80(1): ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  5. ZFYVE26 gene 
    ... ZFYVE26 gene have been found to cause spastic paraplegia type 15. This condition is characterized by progressive movement problems, ... responsible for many of the features of spastic paraplegia type 15.It is unclear whether a lack of spastizin ...
    https://medlineplus.gov/genetics/gene/zfyve26 - Genetics
  6. ATL1 gene 
    ... P, Kremensky I, Mitev V, De Jonghe P. Hereditary spastic paraplegia 3A associated with axonal neuropathy. Arch Neurol. 2007 ... Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegia. Clin Genet. 2011 Jun;79(6):523-30. ...
    https://medlineplus.gov/genetics/gene/atl1 - Genetics
  7. C19orf12 gene 
    ... individuals are considered to have a condition called hereditary spastic paraplegia type 43. More About This Health Condition NBIA3 ... Zuchner S, Blackstone C, Fischbeck KH, Burnett BG. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in ...
    https://medlineplus.gov/genetics/gene/c19orf12 - Genetics