Published 2014
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Spinocerebellar Ataxia 21 with Retardation
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Abstract
Investigators at Universite de Lille Nord de France, and other centers in France, report the identification of a novel causative gene for spinocerebellar ataxia 21, an autosomal dominant disorder, initially mapped to chromosome 7 and designated as SCA21.Files
PNB-2014-28-11-1.pdf
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- PNB-2014-28-11-1
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2014When the item was originally created.