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Showing articles 0 to 4 of 4 Filter Applied: mitochondrial disease (Click to remove) FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018 A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis Neurol 103:e209708, Wannarong,T.,et al, 2024 Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023 Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy Brain 134:3326-3332, Garone, C.,et al, 2011 Showing articles 0 to 4 of 4