
A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2
Keywords: HSP, hereditary spastic paraplegia; PLP1, proteolipid protein 1 (human gene); PMD, Pelizaeus–Merzbacher disease; G, guanosine; C, cytidine; c.88G>C, cDNA nucleotide 88 is changed from guanosine to cytidine; PLP1, proteolipid protein 1 (human protein); kb,