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Results 1 - 10 of 16 for Hereditary spastic paraplegia
  1. WASHC5 gene 
    ... a novel valosin-containing protein binding partner linking hereditary spastic paraplegia to protein aggregation diseases. Brain. 2010 Oct;133( ... PubMed Freeman C, Seaman MN, Reid E. The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  2. SPART gene 
    ... Troyer syndrome. Troyer syndrome is a type of hereditary spastic paraplegia (also called hereditary spastic paraparesis), a group of ... PubMed Lu J, Rashid F, Byrne PC. The hereditary spastic paraplegia protein spartin localises to mitochondria. J Neurochem. 2006 ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  3. 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
  4. SPAST gene 
    ... PubMed SPASTIN; SPAST NCBI Gene ClinVar Blackstone C. Hereditary spastic paraplegia. Handb Clin Neurol. 2018;148:633-652. doi: ... RD. Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin. Nature. 2008 Jan 17;451(7176): ...
    https://medlineplus.gov/genetics/gene/spast - Genetics
  5. REEP1 gene 
    ... Arning L, Epplen JT, Stemmler S. Autosomal dominant hereditary spastic paraplegia: novel mutations in the REEP1 gene (SPG31). BMC ... Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. Am J Hum Genet. 2006 Aug; ...
    https://medlineplus.gov/genetics/gene/reep1 - Genetics
  6. SPG11 gene 
    ... mutations are common in familial cases of complicated hereditary spastic paraplegia. Neurology. 2008 Apr 15;70(16 Pt 2): ... H. Clinical heterogeneity and genotype-phenotype correlations in hereditary spastic paraplegia because of Spatacsin mutations (SPG11). Eur J Neurol. ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  7. SPG7 gene 
    ... deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol. 2003 Nov 24;163(4): ... genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia. Brain. 2004 May;127(Pt 5):973-80. ...
    https://medlineplus.gov/genetics/gene/spg7 - Genetics
  8. 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
  9. CYP7B1 gene 
    ... Bassi MT. Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations. Clin Genet. ... CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5. Brain. 2009 Jun;132(Pt 6): ...
    https://medlineplus.gov/genetics/gene/cyp7b1 - Genetics
  10. GJC2 gene 
    ... Lamantea E, Zeviani M, Scherer SS, Pareyson D. Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations. ...
    https://medlineplus.gov/genetics/gene/gjc2 - Genetics
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