Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations

Solaf M. Elsayed, Raoul Heller, Michaela Thoenes, Maha S. Zaki, Daniel Swan, Ezzat Elsobky, Christine Zühlke, Inga Ebermann, Gudrun Nürnberg, Peter Nürnberg, Hanno J. Bolz*

*Corresponding author for this work
13 Citations (Scopus)

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Medicine & Life Sciences