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Published in 2022 at "Biomolecules"
DOI: 10.3390/biom12081024
Abstract: Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is an inherited neurodegenerative disease characterized by early-onset spasticity in the lower limbs, axonal-demyelinating sensorimotor peripheral neuropathy, and cerebellar ataxia. Our understanding of ARSACS (genetic basis, protein function,…
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Keywords:
based functional;
disease;
integrative organelle;
proteomics silico ... See more keywords