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- W172477297 abstract "Only two SCA13 families, in which KCNC3 mutations have been identified, have been described; very early onset and psychomotor retardation were reported in one of them. PRKCG mutations underlie SCA14, and a number of families have been reported worldwide. SCA14 can manifest with marked extrapyramidal features. Recently, ITPR1 mutations were found in six SCA15 and one SCA16 families with mostly pure cerebellar ataxia." @default.
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- W172477297 date "2010-01-01" @default.
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- W172477297 title "SCA13, 14, 15, and 16" @default.
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- W172477297 doi "https://doi.org/10.1016/b978-0-12-374105-9.00202-1" @default.
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