A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia (Q24301323)

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scientific article published in September 2014
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A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia
scientific article published in September 2014

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    A novel missense mutation in CCDC88C activates the JNK pathway and causes a dominant form of spinocerebellar ataxia (English)
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    September 2014
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