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Academic Journal

Novel UBQLN2 mutations linked to Amyotrophic Lateral Sclerosis and atypical Hereditary Spastic Paraplegia phenotype through defective HSP70-mediated proteolysis

Subjects: Missense/*genetics; Protein Domains/genetics; Mutation

  • Source: ISSN: 0197-4580 ; Neurobiology of Aging ; https://hal.science/hal-03001781 ; Neurobiology of Aging, 2017, 58, pp.239.e11-239.e20. ⟨10.1016/j.neurobiolaging.2017.06.018⟩.

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  • 1-1 ل  1 نتائج ل ""Chartier, Laura""