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机译:Fe / S蛋白组装IBA57基因突变引起遗传性痉挛性截瘫
Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Ophthalmol, Neuroophthalmol Ctr, Jerusalem, Israel;
Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Neurol, Jerusalem, Israel;
Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Genet & Metab Dis, Jerusalem, IsraelShaare Zedek Med Ctr, Dept Neurol, Jerusalem, IsraelUniv Marburg, Inst Zytobiol & Zytopathol, D-35032 Marburg, GermanyHebrew Univ Jerusalem, Hadassah Med Ctr, Dept Radiol, Jerusalem, IsraelUniv Paris 06, Univ Paris 04, Inst Cerveau & Moelle Epiniere, INSERM,U1127,CNRS,UMR7225,UMR 1127Ecole Prat Hautes Etud HeSam Univ, Lab Neurogenet, Inst Cerveau & Moelle Epiniere, Paris, France;
Chromosome 1 Long Arm; maladjustment; protein assemblyencephalomyopathyHereditary Spastic ParaplegiaGenetic Linkage AnalysisMitochondriaMessenger RNAfamily;
机译:Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia
机译:X-linked spastic paraplegia due to a mutation (C506T; Ser169Phe) in exon 4 of the proteolipid protein gene (PLP)
机译:A founder mutation in COQ7, p.(Leu111Pro), causes pure hereditary spastic paraplegia (HSP) in the Iranian population
机译:组蛋白伴侣蛋白Nucleosome Assembly Protein-1(hNAP-1)与HIV-1 Tat结合并促进病毒转录
机译:strumpellin和spartin,Hereditary spastic paraplegia proteins,是Binding partners