December 22, 2017 article Open access SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency Brain DOI: 10.1093/brain/awx369 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 2 stored of 59 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 Biallelic variants in COQ7 cause distal hereditary motor neuropathy with upper motor neuron signs 2023 Brain article Neuroscience Hereditary Neurological Disorders Open access 22 citations Hereditary motor neuropathies 2020 Current Opinion in Neurology article Neuroscience Hereditary Neurological Disorders 11 citations 2 results References 0