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Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
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Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
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Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
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The Ophthalmologic Manifestations of Wilson's Disease
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