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Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay - ScienceDirect
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Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
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IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar
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SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | Human Genetics
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R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram
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A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
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A The SACS gene contains ten exons and spans ~ 104 kb. Graphical view... | Download Scientific Diagram
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Novel frameshift mutation in the SACS gene causing spastic ataxia of charlevoix-saguenay in a consanguineous family from the Arabian Peninsula: A case report and review of literature
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IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish
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Frontiers | Genomic identification of cotton SAC genes branded ovule and stress-related key genes in Gossypium hirsutum
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Insights into SACS pathological attributes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect
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A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
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