![SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram](https://www.researchgate.net/profile/Benjamin_Bender/publication/236052003/figure/fig1/AS:213424647741443@1427895809513/SACS-mutations-Graphical-overview-of-mutations-found-in-this-and-other-studies-Human.png)
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram
![Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts](https://www.mdsabstracts.org/wp-content/uploads/2016/04/551023_lineage.jpg)
Novel variants in the SACS gene in a first Central-Eastern European family with autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) - MDS Abstracts
![Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram](https://www.researchgate.net/profile/Haruo_Shimazaki/publication/224830353/figure/fig2/AS:302759984287750@1449195013621/Primary-structure-of-the-SACS-gene-A-and-domain-organization-of-the-sacsin-protein-B.png)
Primary structure of the SACS gene (A) and domain organization of the... | Download Scientific Diagram
![A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fejhg.2008.58/MediaObjects/41431_2008_Article_BFejhg200858_Fig4_HTML.jpg)
A novel genomic disorder: a deletion of the SACS gene leading to Spastic Ataxia of Charlevoix–Saguenay | European Journal of Human Genetics
![Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family - Palmio - 2016 - Clinical Case Reports - Wiley Online Library Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family - Palmio - 2016 - Clinical Case Reports - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/169aa831-f658-4fe2-8e5c-278828f9e41c/ccr3722-fig-0001-m.jpg)
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix‐Saguenay, ARSACS, in a Finnish family - Palmio - 2016 - Clinical Case Reports - Wiley Online Library
Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay
![Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar Figure 2 from Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Clinical, Radiological and Epidemiological Aspects | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/07db456964438f93bd275e8ac43139d3773edf3c/4-Figure2-1.png)