id	author	title	date	pages	extension	mime	words	sentences	flesch	summary	cache	txt
work_qqtgkcewwzep7gvxe6gxx6bm2i	P A Wilkinson	A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome 12p11.1-12q14	2005.0	3	.pdf	application/pdf	2193	479	71	A new locus for autosomal recessive complicated hereditary spastic paraplegia (SPG26) maps to chromosome he term hereditary spastic paraplegia (HSP) is used to pure forms of the disease, whereas autosomal recessive HSP association with well characterised complicated HSP phenotypes.8 9 Spartin, the protein product of SPG20 mutated in product of the SPG21 gene mutated in Mast syndrome. N The hereditary spastic paraplegias (HSPs) are a Abbreviations: HSP, hereditary spastic paraplegia a novel locus for autosomal recessive complicated HSP to a mutations were identified in affected individuals in any of additional autosomal recessive HSP families for linkage to recessive spastic paraplegias: analysis of 106 patients in 46 families. Spastic paraplegia and OXPHOS impairment caused by mutations in A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia. complicated form of hereditary spastic paraplegia associated with dementia. spastin, mutated in hereditary spastic paraplegia. kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia	./cache/work_qqtgkcewwzep7gvxe6gxx6bm2i.pdf	./txt/work_qqtgkcewwzep7gvxe6gxx6bm2i.txt