Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia
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E. Bertini | C. Pignata | A. Capuano | G. Zanni | M. Nardella | E. Bellacchio | F. Nicita | P. Alfieri | G. Terrone | G. Piccini | Federica Graziola