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schraper ontsnapping uit de gevangenis Oraal sacs gene Gecomprimeerd Kameraad Vervoer

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

Novel compound heterozygous mutations of the SACS gene in autosomal  recessive spastic ataxia of Charlevoix-Saguenay - ScienceDirect
Novel compound heterozygous mutations of the SACS gene in autosomal recessive spastic ataxia of Charlevoix-Saguenay - ScienceDirect

SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody

IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of  Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration

IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related  Disease Phenotypes in Zebrafish
IJMS | Free Full-Text | Efficient Neuroprotective Rescue of Sacsin-Related Disease Phenotypes in Zebrafish

Insights into SACS pathological attributes in autosomal recessive spastic  ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect
Insights into SACS pathological attributes in autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS)☆ - ScienceDirect

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: Compound  Heterozygotes for Nonsense Mutations of the SACS Gene - Vinodh Narayanan,  Stephen G. Rice, Shannon S. Olfers, Kumaraswamy Sivakumar, 2011
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay: Compound Heterozygotes for Nonsense Mutations of the SACS Gene - Vinodh Narayanan, Stephen G. Rice, Shannon S. Olfers, Kumaraswamy Sivakumar, 2011

ARSACS: Genetics and More - 23andMe
ARSACS: Genetics and More - 23andMe

Frontiers | Genomic identification of cotton SAC genes branded ovule and  stress-related key genes in Gossypium hirsutum
Frontiers | Genomic identification of cotton SAC genes branded ovule and stress-related key genes in Gossypium hirsutum

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
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

Sacsin - Wikipedia
Sacsin - Wikipedia

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

Sacsin cotranslational degradation causes autosomal recessive spastic  ataxia of Charlevoix-Saguenay | bioRxiv
Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay | bioRxiv

SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay | ACNR Journal

ARSACS DNA Test – DNA Access Lab
ARSACS DNA Test – DNA Access Lab

SACS gene
SACS gene

R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... |  Download Scientific Diagram
R272C Sacs knock-in mice. (a) Schematic representation of mouse sacsin... | Download Scientific Diagram

SACS Gene - GeneCards | SACS Protein | SACS Antibody
SACS Gene - GeneCards | SACS Protein | SACS Antibody

SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients
SACS Gene Associated With CMT-Like Disease in Two Brazilian Patients

SACS variants are a relevant cause of autosomal recessive hereditary motor  and sensory neuropathy | Human Genetics
SACS variants are a relevant cause of autosomal recessive hereditary motor and sensory neuropathy | Human Genetics

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

IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of  Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration
IJMS | Free Full-Text | Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration

RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M
RCSB PDB - 5VSZ: Structure of the Ubl domain of Sacsin mutant L78M