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Oxford University Press

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A new autosomal recessive non-progressive congenital cerebellar ataxia associated with mental retardation, optic atrophy, and skin abnormalities (CAMOS) maps to chromosome 15q24-q26 in a large consanguineous Lebanese Druze family

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Retinal Imaging in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

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Autosomal recessive spinocerebellar ataxia and peripheral neuropathy with raised α-fetoprotein

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