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Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia

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Description scientific article published on 30 November 2016
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author: Marta Nardella  Massimiliano Valeriani  José M Fernández-Fernández  Raffaella Cusmai  Lorena Travaglini  Sabina Barresi  Roberto Frusciante  Nicola Specchio  Emanuele Bellacchio  Federico Vigevano  Alessandro Capuano  Ginevra Zanni  Enrico Bertini 

Publication date November 30, 2016
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