April 19, 2021 article Open access Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients Scientific Reports DOI: 10.1038/s41598-021-86857-0 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 4 stored of 27 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access When muscles matter in SORD neuropathy 2026 Journal of Neuropathology & Experimental Neurology article Neuroscience Hereditary Neurological Disorders 0 citations Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD 2025 Brain article Neuroscience Hereditary Neurological Disorders Open access 12 citations SORD-deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights 2024 Brain article Neuroscience Hereditary Neurological Disorders Open access 10 citations Sord deficient rats develop a motor-predominant peripheral neuropathy unveiling novel pathophysiological insights 2023 bioRxiv (Cold Spring Harbor Laboratory) preprint Neuroscience Hereditary Neurological Disorders Open access 2 citations 4 results References 0