...
机译:常染色体隐性纯的小说形式遗传性痉挛性截瘫映射到染色体13 q14。
Genetics Department, King Faisal Specialist Hospital and Research Centre Riyadh, Kingdom of Saudi Arabia. hodgkinson@kfshrc.edu.sa;
Recessive; Spastic Paraplegia; Pure hereditary spastic paraplegiaLower limb spasticityChromosomes13q14vif GenesAutosomeMicrosatellite Repeats;
机译:SPTAN1 variants likely cause autosomal recessive complicated hereditary spastic paraplegia
机译:MYO1H is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia
机译:Genetic anticipation in a large family with pure autosomal dominant hereditary spastic paraplegia
机译:strumpellin和spartin,Hereditary spastic paraplegia proteins,是Binding partners