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A novel mutation in SACS gene in a family from southern Italy
PDF] Autosomal recessive spastic ataxia of Charlevoix-Saguenay in a Portuguese child caused by a novel SACS mutation | Semantic Scholar
Sacs R272C missense homozygous mice develop an ataxia phenotype | Molecular Brain | Full Text
SACS Gene - GeneCards | SACS Protein | SACS Antibody
Insights into SACS pathological attributes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect
SACS gene
Sacsin - Wikipedia
Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families - ScienceDirect
Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsinin Neurodegeneration
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
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
Sacsin - Wikipedia
Mutation in the SACS gene in the pathogenesis of ARSACS. An absence or... | Download Scientific Diagram
ARSACS DNA Test – DNA Access Lab
SACS mutations. Graphical overview of mutations found in this and other... | Download Scientific Diagram