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Complex Ataxia
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Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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A Young Woman with Rapid Mental Deterioration and Leukoencephalopathy
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
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Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and KCNJ10 Mutations
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Genetic Counseling in Retinitis Pigmentosa
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