Sequence variants in SPAST, SPG3A and HSPD1 in hereditary spastic paraplegia
Journal of the neurological sciences, Volume 284, Issue 1-2, 2009, Pages 90-95.
Hereditary spastic paraplegia (HSP) is a group of clinically and genetically heterogeneous neurodegenerative disorders characterized by progressive spasticity and weakness in the lower limbs. The most common forms of autosomal dominant HSP, SPG4 and SPG3, are caused by sequence variants in the SPAST and SPG3A genes, respectively. The path...More
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