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Dive into the research topics of 'Autosomal dominant SCA5 and autosomal recessive infantile SCA are allelic conditions resulting from SPTBN2 mutations'. Together they form a unique fingerprint.- Sort by
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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*