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Results 1 - 5 of 5 for Complex hereditary spastic paraplegia
  1. CYP7B1 gene 
    ... A, Stevanin G. 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
  2. SPART gene 
    ... Brown NA, Crosby AH. Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons. Exp ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  3. SPG7 gene 
    ... Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol. 2003 Nov 24;163(4): ...
    https://medlineplus.gov/genetics/gene/spg7 - Genetics
  4. WASHC5 gene 
    ... PubMed Freeman C, Seaman MN, Reid E. The hereditary spastic paraplegia protein strumpellin: characterisation in neurons and of the effect of disease mutations on WASH complex assembly and function. Biochim Biophys Acta. 2013 Jan; ...
    https://medlineplus.gov/genetics/gene/washc5 - Genetics
  5. TECPR2 gene 
    ... family trio suggests involvement of TECPR2 in a complex form of progressive motor neuron disease. Clin Genet. ... cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability. Eur J ...
    https://medlineplus.gov/genetics/gene/tecpr2 - Genetics