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Melas Syndrome
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Spinal Muscular Atrophy
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Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
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Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Clinical Spectrum of CADASIL:A Study of 7 Families
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