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Results 11 - 16 of 16 for Complex hereditary spastic paraplegia
  1. 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
  2. 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
  3. Spastic paraplegia type 8 
    ... 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/condition/spastic-paraplegia-type-8 - 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. Spastic paraplegia type 2 
    ... the development of paralysis of the lower limbs (paraplegia). Hereditary spastic paraplegias are divided into two types: pure and complex. The pure types involve the lower limbs. The ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
  6. 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
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