(Q37493127)
Statements
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Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations (English)
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Peter Nürnberg
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Raoul Heller
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Michaela Thoenes
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Ezzat Elsobky
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Inga Ebermann
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Hanno J Bolz
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10 July 2013
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286-288
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Identifiers
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