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Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
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De Novo Mutation in the Notch3 Gene Causing CADASIL
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Retinocochleocerebral Vasculopathy
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Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
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