Associated Papers
A Novel SACS Variant Identified in a Chinese Patient: Case Report and Review of the Literature.
Chen Y et al.
Frontiers in Neurology, 2022
Genetic spectrum and clinical features in a cohort of Chinese patients with autosomal recessive cerebellar ataxias.
Cheng HL et al.
Translational Neurodegeneration, 2021
34663476 (PubMed )
Supplement: 40035_2021_264_MOESM4_ESM.xlsx › Table_S2
A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.
Zeng H et al.
Cytogenetic and Genome Research, 2017
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